Flu Fix NDC 69676-0010

NDC codes

FDA NDC Directory

Product NDC (as listed)69676-0010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69676-0010Add 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
69676-0010-1	69676001001	1 BOTTLE, PLASTIC in 1 CARTON (69676-0010-1) / 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTICMarketed from Jul 11, 2018

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): Flu Fix
Generic name (nonproprietary): aconitum napellus, allium cepa, anis barbariae, bryonia alba, echinacea angustifolia, eupatorium perfollatum, gelsemium sempervirens, ipecacauanha, nux vomica, pulsatilla, rhus toxicodendron
Active ingredients: Strychnos nux-vomica seed — 12 [hp_X]/1Eupatorium perfoliatum flowering top — 6 [hp_X]/1Gelsemium sempervirens root — 12 [hp_X]/1Pulsatilla pratensis — 9 [hp_X]/1Toxicodendron pubescens shoot — 12 [hp_X]/1Onion — 6 [hp_X]/1Bryonia alba root — 9 [hp_X]/1Echinacea angustifolia — 6 [hp_X]/1Aconitum napellus — 12 [hp_X]/1Euphrasia stricta — 6 [hp_X]/1Cairina moschata heart/liver autolysate — 6 [hp_C]/1Ipecac — 12 [hp_X]/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: Genexa Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 11, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 69676-0010_5a37a5d6-6dfd-fdcd-e063-6394a90a7a21SPL ID 5a37a5d6-6dfd-fdcd-e063-6394a90a7a21SPL set ID 7900b6f2-a563-831c-e053-2a91aa0a558dUNII 269XH13919, 1W0775VX6E, 639KR60Q1Q, 8E272251DI, 46PYZ1F82M, 492225Q21H, T7J046YI2B, VB06AV5US8, U0NQ8555JD, C9642I91WL, RN2HC612GY, 62I3C8233L
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N469676001001 followed by a unit qualifier and the quantity

Package 69676-0010-01. 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 Aug 29, 2026.

Indications (excerpt from the label)

Uses* addresses symptoms associated with the flu, such as: body aches headache chills fatigue congestion sore throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)