NDC codes

FDA NDC Directory
Product NDC (as listed)43742-1561Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43742-1561Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
43742-1561-1437421561014374215610130 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

N443742156101 followed by a unit qualifier and the quantity

Package 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.

Full label on DailyMed (opens in a new tab)

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.

Other finished products listed under the same name: strengths, forms and labelers.

Other Free Radical NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage 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 metallicumAcetaldehyde 30 [hp_X]/mL + 26 more ingredientsLiquidOralDeseret Biologicals, Inc.43742-254943742-2549-01
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, bromiumTriticum aestivum whole 1 [hp_X]/mL + 66 more ingredientsLiquidOralBioActive Nutritional, Inc.43857-048143857-0481-01

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