Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Free Radical NDC 43742-1561
Medicago sativa whole 6 [hp_X]/mL + 26 more ingredients · Liquid · Oral · Deseret Biologicals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43742-1561-1 | 4374215610143742156101 | 30 mL in 1 BOTTLE, DROPPER (43742-1561-1)Marketed from Sep 6, 2019 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Free Radical
- Generic name (nonproprietary)
- alfalfa, ascorbyl palmitate, cysteinum, dimethyl glycine, fucus vesiculosus, hordeum vulgare, l-methionine, manganese gluconate, nasturtium aquaticum, quercetin, raphanus sativus, sodium selenite, triticum aestivum, ubidecarenonum, alpha-lipoicum acidum, gaba (gamma aminobutyric acid), oryza sativa, vitamin e, zinc picolinate, cobaltum metallicum, ferrum metallicum, glutathione, magnesium fluoratum, selenium metallicum, zincum metallicum, alpha-ketoglutaricum acidum
- Active ingredients
- Medicago sativa whole — 6 [hp_X]/mLAscorbyl palmitate — 6 [hp_X]/mLCysteine — 6 [hp_X]/mLN,N-dimethylglycine — 6 [hp_X]/mLFucus vesiculosus — 6 [hp_X]/mLBarley — 6 [hp_X]/mLMethionine — 6 [hp_X]/mLManganese gluconate — 6 [hp_X]/mLNasturtium officinale — 6 [hp_X]/mLQuercetin — 6 [hp_X]/mLRaphanus sativus — 6 [hp_X]/mLSodium selenite — 6 [hp_X]/mLWheat — 6 [hp_X]/mLUbidecarenone — 6 [hp_X]/mL.alpha.-lipoic acid — 8 [hp_X]/mL.gamma.-aminobutyric acid — 8 [hp_X]/mLOryza sativa whole — 8 [hp_X]/mL.alpha.-tocopherol — 8 [hp_X]/mLZinc picolinate — 8 [hp_X]/mLCobalt — 12 [hp_X]/mLIron — 12 [hp_X]/mLGlutathione — 12 [hp_X]/mLMagnesium fluoride — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLZinc — 12 [hp_X]/mLAcetaldehyde — 30 [hp_X]/mL.alpha.-ketoglutaric acid — 30 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Deseret Biologicals, Inc.NDC labeler code 43742
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Marketing end
- Other FDA classes
- Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Grain Proteins (EXT)Grain Proteins (EXT)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)
- Identifiers
- Product ID 43742-1561_4a4c582e-202a-46d3-ad52-9127f1752e3cSPL ID 4a4c582e-202a-46d3-ad52-9127f1752e3cSPL set ID 36060680-f0d2-44c3-82fa-649e6e9d454dUNII DJO934BRBD, QN83US2B0N, K848JZ4886, 7797M4CPPA, 535G2ABX9M, 5PWM7YLI7R, AE28F7PNPL, 9YY2F980SV, YH89GMV676, 9IKM0I5T1E, 86R5J6D01D, HIW548RQ3W, 4J2I0SN84Y, EJ27X76M46, 73Y7P0K73Y, 2ACZ6IPC6I, 84IVV0906Z, H4N855PNZ1, ALO92O31SE, 3G0H8C9362, E1UOL152H7, GAN16C9B8O, 5N014C7IWU, H6241UJ22B, J41CSQ7QDS, GO1N1ZPR3B, 8ID597Z82X
- Pharmacologic class
- Copper Absorption Inhibitor; Non-Standardized Food Allergenic Extract; Paramagnetic Contrast Agent; Standardized Chemical Allergen
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N443742156101followed by a unit qualifier and the quantityPackage 43742-1561-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
USES: • For the temporary relief of symptoms including: • tingling in hands • tingling in feet • mood changes • frequent colds • poor digestion • fatigue • occasional constipation These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Excerpt only. Read the full label for complete information.
About NDC 43742-1561
- What is NDC 43742-1561?
- 43742-1561 is the product NDC for Free Radical, Medicago sativa whole 6 [hp_X]/mL + 26 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Free Radical (Alfalfa, Ascorbyl Palmitate, Cysteinum, Dimethyl Glycine, Fucus Vesiculosus, Hordeum Vulgare, L-Methionine, Manganese Gluconate, Nasturtium Aquaticum, Quercetin, Raphanus Sativus, Sodium Selenite, Triticum Aestivum, Ubidecarenonum, alpha-Lipoicum Acidum, GABA (Gamma Aminobutyric Acid), Oryza Sativa, Vitamin E, Zinc Picolinate, Cobaltum Metallicum, Ferrum Metallicum, Glutathione, Magnesium Fluoratum, Selenium Metallicum, Zincum Metallicum, alpha-Ketoglutaricum Acidum).
- What is the active ingredient?
- Medicago sativa whole, Ascorbyl palmitate, Cysteine, N,N-dimethylglycine, Fucus vesiculosus, Barley, Methionine, Manganese gluconate, Nasturtium officinale, Quercetin, Raphanus sativus, Sodium selenite, Wheat, Ubidecarenone, .alpha.-lipoic acid, .gamma.-aminobutyric acid, Oryza sativa whole, .alpha.-tocopherol, Zinc picolinate, Cobalt, Iron, Glutathione, Magnesium fluoride, Selenium, Zinc, Acetaldehyde, .alpha.-ketoglutaric acid.
- Who is the labeler?
- Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Free Radical?
- 2 other product NDCs are listed under this name. See all Free Radical NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Free Radical products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Free Radicalacetaldehyde, alfalfa, alpha-ketoglutaricum acidum, alpha-lipoicum acidum, ascorbyl palmitate, cobaltum metallicum, cysteinum, dimethyl glycine, ferrum metallicum, fucus vesiculosus, gaba (gamma aminobutyric acid), glutathione, hordeum vulgare, l-methionine, magnesium fluoratum, manganese gluconate, nasturtium aquaticum, oryza sativa, quercetin, raphanus sativus, selenium metallicum, sodium selenite, triticum aestivum, ubidecarenonum, vitamin e, zinc picolinate, zincum metallicum | Acetaldehyde 30 [hp_X]/mL + 26 more ingredients | LiquidOral | Deseret Biologicals, Inc. | 43742-2549 | 43742-2549-01 |
| Free Radicaltriticum aestivum, alfalfa, fucus vesiculosus, laminaria digitata, nasturtium aquaticum, oryza sativa, raphanus sativus, symphytum officinale, hordeum vulgare, asparagus officinalis, manganese gluconate, ferrum phosphoricum, arnica montana, cuprum metallicum, ubidecarenonum, alpha-ketoglutaricum acidum, glyoxal trimer dihydrate, aluminum metallicum, antimonium crudum, argentum metallicum, arsenicum album, aurum metallicum, baryta carbonica, beryllium metallicum, bismuthum metallicum, boron, bromium | Triticum aestivum whole 1 [hp_X]/mL + 66 more ingredients | LiquidOral | BioActive Nutritional, Inc. | 43857-0481 | 43857-0481-01 |