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Biogena Multispectrum 24/7® Active Juice
Multivitamin / basic supply · ml

Biogena Multispectrum 24/7® Active Juice

250 ml · 5–10 ml per day

List price31.90 €250 ml
Price/day0.64–1.28 €
Supply25–50 days
25 € discount
Code AD1131373
from 75 € order value
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Current product/batch-specific notice: If taking anticoagulants, consult a doctor in advance because the product contains vitamin K. Contains xylitol. After opening, store refrigerated, shake before use and consume within eight weeks. (checked 16 Sep 2026)

Product description

Liquid multi-nutrient product with magnesium, vitamins C, D3, E and K2, B vitamins, zinc, selenium, iodine and other micronutrients. Dosage is 5 ml for ages 4–9 and 10 ml from age 10.

Checked: 16 Sep 2026• Ingredients list complete• Lab report available• without MCC• without silicon dioxide
Editorial assessment

Assessment by Oliver Fröhner

Micronutrient expert & Food Coach

Product character

The juice is a broad multi-nutrient formula and should not be assessed by a single ingredient. The structured 10 ml reference dose corresponds to the manufacturer's dose for children from age 10 and adults.

Formula & transparency

  • Ingredients list fully checked
  • Without microcrystalline cellulose according to the fully reviewed ingredient list
  • Without silicon dioxide according to the fully reviewed ingredient list
  • Product data reviewed within the freshness period

Points to consider

  • A current product- or batch-specific notice is available.

Data basis

  • Lab report available but not marked as reviewed

Summary by Oliver Fröhner

Liquid multi-nutrient product with magnesium, vitamins C, D3, E and K2, B vitamins, zinc, selenium, iodine and other micronutrients. Dosage is 5 ml for ages 4–9 and 10 ml from age 10.

Manufacturer information and Oliver Fröhner’s editorial assessment are presented separately. Data checked: 16 Sep 2026.

Active ingredients & NRV

Active ingredients

Vitamin D3 — 20 µg · per Daily dose400 % NRV
Zinc — 8 mg · per Daily dose80 % NRV
Vitamin K2 — 40 µg · per Daily dose53 % NRV
Vitamin A — 400 µg · per Daily dose50 % NRV
Vitamin B12 — 3 µg · per Daily dose120 % NRV
Biotin — 40 µg · per Daily dose80 % NRV
Niacin — 16 mg · per Daily dose100 % NRV
Vitamin E — 20 mg · per Daily dose167 % NRV
Vitamin B6 — 1.4 mg · per Daily dose100 % NRV
Selenium — 60 µg · per Daily dose109 % NRV
Pantothenic Acid — 6 mg · per Daily dose100 % NRV
Vitamin B2 — 1.8 mg · per Daily dose129 % NRV
Vitamin C — 120 mg · per Daily dose150 % NRV
Iodine — 100 µg · per Daily dose67 % NRV
Folate — 200 µg · per Daily dose100 % NRV
Magnesium — 56 mg · per Daily dose15 % NRV
Vitamin B1 — 1.6 mg · per Daily dose145 % NRV
Ingredients & additives

Wasser, Süßungsmittel: Xylit; Magnesiumcitrat, Apfelfruchtsaftpulver (4,3 %), Pfirsichfruchtsaftpulver (4,3 %), L-Ascorbinsäure, Maltodextrin, D-alpha-Tocopherylacetat, Zinkcitrat, Verdickungsmittel: Xanthan; Nicotinamid, Konservierungsstoff: Kaliumsorbat; Calcium-D-pantothenat, Retinylacetat, natürliches Pfirsicharoma, Thiaminmononitrat, Riboflavin, Pyridoxinhydrochlorid, Cholecalciferol, Folsäure, Natriumselenat, Kaliumiodid, D-Biotin, Vitamin K2 (Menachinon-7), Methylcobalamin.

without MCC without SiO₂
Directions & package

Children aged 4–9 years: 5 ml daily. Children aged 10 years and older and adults: 10 ml daily. Shake before use.

250 ml · 25–50 days

Quality, lab & sources

Lab status: Lab report available

Product data checked on 16 Sep 2026.

Notes

If taking anticoagulants, consult a doctor in advance because the product contains vitamin K. Contains xylitol. After opening, store refrigerated, shake before use and consume within eight weeks.

Nutrient knowledge & reference values

Nutrient knowledge & reference values

General nutrient information for interpreting the product dosage. Signs of insufficient or excessive intake are non-specific and do not replace a diagnosis.

Vitamin D3

Vitamin D is a fat-soluble vitamin and also a precursor of hormonally active metabolites. For the assessment of supplements, product dose, dosing interval, total intake, 25-OH-vitamin-D status and safety limits are considered separately.

NRV 200 IE European Union · 2011 EU NRV: 5 µg vitamin D, equivalent to 200 IU. Labelling reference value; not a therapeutic target and not a safety limit. Source →
UL 4,000 IE EFSA · EFSA current EFSA UL: 100 µg vitamin D per day, equivalent to 4,000 IU. Safety limit for long-term intake, not an optimal target value. Source →
UL 4,000 IE US FNB / NASEM (NIH ODS) · NIH ODS current US UL: 100 µg or 4,000 IU of vitamin D per day for adults. Safety limit, not a target value. Source →

Functions

EU-authorised functions include, among other things: vitamin D contributes to normal absorption and utilisation of calcium and phosphorus, normal blood calcium levels, the maintenance of normal bones and teeth, normal muscle function and normal functioning of the immune system. Vitamin D also has a role in the process of cell division.

Possible signs of insufficient intake

Inadequate vitamin D status cannot be reliably identified from individual nonspecific symptoms. For individual assessment, 25-OH-vitamin-D status together with exposure, diet and supplemental intake is more informative than symptoms alone.

Points to consider at high intake

A markedly excessive vitamin D intake over a prolonged period can lead to hypercalcaemia and hypercalciuria and thereby place a burden on the kidneys and other organ systems. Upper Intake Levels are safety limits for long-term intake and are not optimal target values.

Special considerations

Particular caution is required, among other situations, with diseases or therapies that affect calcium metabolism or kidney function. High doses should not be derived solely from general target values.

Interactions / caution

Vitamin D can interact with certain medicines; relevant examples include drugs that affect calcium or vitamin D metabolism. With prolonged higher-dose use, individual medication should be taken into account.

Knowledge reviewed on 23 Sep 2026

Zinc

Zinc is an essential trace element. The assessment considers the EU NRV, total intake, product dose and interactions—particularly with copper and medicines—separately.

NRV 10 mg European Union · 2011 Product daily dose: 80 % of the reference value EU NRV for nutrition labelling; not a therapeutic target and not a safety limit. Source →
UL 25 mg EFSA / SCF · 2002 / EFSA Summary 2024 Safety limit for long-term intake; not a target value. Source →
UL 40 mg US FNB / NASEM (NIH ODS) · NIH ODS current Product daily dose: 20 % of the UL; other intake sources are not included. US UL for zinc from all sources. Safety limit, not a target value. Source →

Functions

EU-authorised health-claim functions include, among other things: zinc contributes to the normal function of the immune system, normal cognitive function, normal DNA synthesis, normal fertility and reproduction, and normal acid-base and carbohydrate metabolism. Zinc contributes to the maintenance of normal bones, hair, nails, skin and vision, protects cells from oxidative stress and has a role in the process of cell division.

Possible signs of insufficient intake

Zinc deficiency can be associated, among other things, with loss of appetite, impaired taste and smell, delayed wound healing, hair loss, growth impairment and increased susceptibility to infections. These symptoms are nonspecific and do not allow self-diagnosis.

Points to consider at high intake

Excessive zinc intake can cause nausea, vomiting, headaches and gastrointestinal symptoms. Chronically high amounts can inhibit copper absorption and thereby promote copper deficiency. The European EFSA/SCF UL for adults is 25 mg of zinc per day from total intake.

Special considerations

An increased risk of inadequate zinc intake exists, among other situations, with certain gastrointestinal diseases or after bariatric surgery, with strongly plant-based diets with low zinc bioavailability, during pregnancy and breastfeeding, and with chronically high alcohol consumption.

Interactions / caution

Zinc can reduce the absorption of quinolone and tetracycline antibiotics as well as penicillamine; dosing intervals should be observed. Thiazide diuretics can increase zinc excretion. Long-term high zinc intake can reduce copper absorption.

Knowledge reviewed on 23 Sep 2026

Vitamin K2

Vitamin K2 belongs to the vitamin K family and includes various menaquinones such as MK-4 and MK-7. MK-7 is commonly used in food supplements. K1 and K2 should not be treated as generally equivalent, even though the authorised vitamin K functions apply to vitamin K as a whole.

Functions

EU-authorised functions: Vitamin K contributes to normal blood clotting and to the maintenance of normal bones.

Possible signs of insufficient intake

Insufficient vitamin K status can impair vitamin-K-dependent blood clotting. An individual assessment should not be based solely on nonspecific symptoms.

Points to consider at high intake

No numerical US UL has been established for vitamin K because of insufficient data and the comparatively low observed toxicity. This does not mean that unlimited dosing is safe, particularly in the presence of relevant medication.

Special considerations

Particular attention is required in people taking vitamin-K-antagonist anticoagulants. In this context, independently changing vitamin K intake is not advisable.

Interactions / caution

Vitamin K can interact clinically significantly with vitamin K antagonists such as warfarin, phenprocoumon and similar anticoagulants. During such therapy, vitamin K intake should only be changed in consultation with the treating medical team.

Knowledge reviewed on 23 Sep 2026

Vitamin A

UL 3,000 µg US FNB / NASEM (NIH ODS) · NIH ODS current UL applies only to preformed vitamin A from retinol or retinyl esters such as retinyl palmitate, not to beta-carotene/provitamin A carotenoids. Compare only when the product form is clearly identified. Source →

Vitamin B6

UL 12 mg EFSA · 2023 Product daily dose: 12 % of the UL; other intake sources are not included. EFSA UL 12 mg/day for adults; includes total intake from foods and supplements and all vitamin B6 vitamers. Safety limit, not a target value. Source →
UL 100 mg US FNB / NASEM (NIH ODS) · NIH ODS current Product daily dose: 1 % of the UL; other intake sources are not included. US UL 100 mg/day for adults from food and supplement sources. Considerably higher than the EFSA UL newly derived in 2023; note the different derivation methods. Source →

Selenium

Selenium is an essential trace element. Product dosage, selenium form, reference values and total intake are considered separately in the assessment.

NRV 55 µg European Union · 2011 Product daily dose: 109 % of the reference value EU NRV for nutrition labelling; not a therapeutic target and not a safety limit. Source →
UL 255 µg EFSA · 2023 Product daily dose: 24 % of the UL; other intake sources are not included. UL for long-term total intake in adults; safety limit, not a target value. Source →
UL 400 µg US FNB / NASEM (NIH ODS) · NIH ODS current Product daily dose: 15 % of the UL; other intake sources are not included. US UL for selenium from food and supplements. Safety limit, not a target value. Source →

Functions

Selenium is a component of various selenoproteins and plays a role, among other things, in antioxidant defence systems, the regulation of thyroid-hormone metabolism and normal immune-system function.

Possible signs of insufficient intake

Insufficient selenium intake can impair various selenium-dependent enzyme systems. Symptoms are nonspecific; for an individual assessment, diet, supplemental intake and, where appropriate, laboratory parameters should be considered together.

Points to consider at high intake

Chronically high selenium intake can lead to selenosis. Reported signs include changes in hair and nails, a metallic taste, garlic-like breath, as well as gastrointestinal and neurological symptoms.

Special considerations

Baseline selenium status is particularly relevant when interpreting selenium studies. High additional intake is not automatically beneficial when selenium status is already adequate.

Interactions / caution

With high-dose long-term use, total intake from food and supplements should be taken into account. Individual medical conditions and drug therapies may require a separate assessment.

Knowledge reviewed on 23 Sep 2026

Vitamin C

Vitamin C (ascorbic acid) is an essential water-soluble vitamin. presents physiological functions, the EU NRV, safety assessment and product-specific dosage separately.

NRV 80 mg European Union · 2011 Product daily dose: 150 % of the reference value EU NRV for nutrition labelling; not a therapeutic target and not a safety limit. Source →
UL 2,000 mg US FNB / NASEM (NIH ODS) · NIH ODS current Product daily dose: 6 % of the UL; other intake sources are not included. US UL for vitamin C from food and supplements. Safety limit, not a target value. Source →

Functions

EU-authorised health-claim functions include, among other things: vitamin C contributes to normal collagen formation for the normal function of blood vessels, bones, cartilage, gums, skin and teeth. It contributes to normal energy-yielding metabolism, normal functioning of the nervous system and immune system, and the protection of cells from oxidative stress. Vitamin C also contributes to the reduction of tiredness and fatigue and increases iron absorption.

Possible signs of insufficient intake

Severe vitamin C deficiency can lead to scurvy. Reported signs include fatigue, inflammation of the gums, pinpoint bleeding, increased capillary fragility and delayed wound healing. Such symptoms are not suitable for self-diagnosis.

Points to consider at high intake

EFSA was unable to derive a UL for vitamin C because of insufficient data. High additional intake can mainly cause gastrointestinal symptoms such as diarrhoea, nausea, bloating or abdominal cramps. With very high amounts, individual risk factors should be taken into account.

Special considerations

An increased risk of inadequate intake exists, among other situations, with a very one-sided diet, malabsorption and in smokers or people with substantial passive-smoke exposure. In haemochromatosis, particular caution is advisable with high-dose vitamin C because it increases non-haem iron absorption.

Interactions / caution

Vitamin C can increase non-haem iron absorption. High-dose supplementation in haemochromatosis should only be used after professional consultation. During chemotherapy or radiotherapy, high-dose antioxidant supplementation should be coordinated with the treating team.

Knowledge reviewed on 23 Sep 2026

Magnesium

Magnesium is an essential mineral involved in numerous enzymatic reactions. For product assessment, the manufacturer’s dosage, active-ingredient forms and reference values are considered separately.

NRV 375 mg European Union · 2011 Product daily dose: 15 % of the reference value EU NRV for nutrition labelling; not a therapeutic target and not a safety limit. Source →
UL 250 mg EFSA / SCF · 2001 / EFSA Summary 2024 Product daily dose: 22 % of the UL; other intake sources are not included. UL for readily dissociable magnesium salts/magnesium oxide from food supplements or other added sources; naturally occurring magnesium from foods is not covered in the same way. Source →
UL 350 mg US FNB / NASEM (NIH ODS) · NIH ODS current Product daily dose: 16 % of the UL; other intake sources are not included. The US UL covers magnesium from dietary supplements and medicines, not magnesium naturally present in foods and beverages. Safety limit, not a target value. Source →

Functions

Magnesium contributes, among other things, to normal muscle and nerve function and to normal energy-yielding metabolic processes. It is also involved in processes related to protein, bone and DNA.

Possible signs of insufficient intake

Insufficient magnesium intake can present with nonspecific symptoms; possible indications may include neuromuscular complaints. Individual symptoms do not establish a diagnosis and should not be assessed in isolation.

Points to consider at high intake

High amounts from supplements can mainly cause gastrointestinal symptoms such as diarrhoea, nausea and abdominal cramps. With severely impaired kidney function, the risk of magnesium accumulation increases; high doses should then be medically assessed.

Special considerations

With impaired kidney function, magnesium excretion is reduced. Product dose, magnesium form, tolerance and total intake should therefore be considered separately.

Interactions / caution

Magnesium can affect the absorption of certain medicines, including some antibiotics and bisphosphonates. Timing intervals and individual medication should be reviewed with regular use.

Knowledge reviewed on 23 Sep 2026
Science & studies

Scientific assessment

Studies, meta-analyses and randomized controlled trials on the active ingredient – explained clearly and linked to sources.

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The information is provided for factual classification of product and nutrient data. It does not replace medical diagnosis or individual treatment advice.

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