Free Radical NDC 43742-2549

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2549Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2549Add 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 NDC	11-digit (billing)	Package	Copy
43742-2549-1	43742254901	30 mL in 1 BOTTLE, DROPPER (43742-2549-1)Marketed from Jun 2, 2026

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): acetaldehyde, 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
Active ingredients: Acetaldehyde — 30 [hp_X]/mLMedicago sativa whole — 6 [hp_X]/mLOxogluric acid — 30 [hp_X]/mLAlpha lipoic acid — 8 [hp_X]/mLAscorbyl palmitate — 6 [hp_X]/mLCobalt — 12 [hp_X]/mLCysteine — 6 [hp_X]/mLN,N-dimethylglycine — 6 [hp_X]/mLIron — 12 [hp_X]/mLFucus vesiculosus — 12 [hp_X]/mL.gamma.-aminobutyric acid — 8 [hp_X]/mLGlutathione — 12 [hp_X]/mLHordeum vulgare top — 6 [hp_X]/mLMethionine — 6 [hp_X]/mLMagnesium fluoride — 30 [hp_X]/mLManganese gluconate, Unspecified form — 6 [hp_X]/mLNasturtium officinale — 6 [hp_X]/mLBrown rice — 8 [hp_X]/mLQuercetin — 6 [hp_X]/mLRadish — 6 [hp_X]/mLSelenium — 12 [hp_X]/mLSodium selenite — 6 [hp_X]/mLTriticum aestivum whole — 6 [hp_X]/mLUbidecarenone — 6 [hp_X]/mL.alpha.-tocopherol — 8 [hp_X]/mLZinc picolinate — 8 [hp_X]/mLZinc — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 2, 2026
Listing expires: Dec 31, 2027
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)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 43742-2549_2223706f-ccd6-4580-becd-085534352a4dSPL ID 2223706f-ccd6-4580-becd-085534352a4dSPL set ID 2408a38a-9cdd-48c0-b76c-b72e4fe5d719UNII GO1N1ZPR3B, DJO934BRBD, 8ID597Z82X, 73Y7P0K73Y, QN83US2B0N, 3G0H8C9362, K848JZ4886, 7797M4CPPA, E1UOL152H7, 535G2ABX9M, 2ACZ6IPC6I, GAN16C9B8O, 86507VZR9K, AE28F7PNPL, 5N014C7IWU, 9YY2F980SV, YH89GMV676, 659G217HPG, 9IKM0I5T1E, EM5RP35463, H6241UJ22B, HIW548RQ3W, 3C3Y389JBU, EJ27X76M46, H4N855PNZ1, ALO92O31SE, J41CSQ7QDS
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

N443742254901 followed by a unit qualifier and the quantity

Package 43742-2549-01. 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 Jun 2, 2026.

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)