Guna Flam Relief NDC 17089-464

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-464Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0464Add 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
17089-464-18	17089046418	1 BOTTLE, DROPPER in 1 BOX (17089-464-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Sep 24, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Guna Flam Relief
Generic name (nonproprietary): aconitum napellus - apis mellifera - arnica montana whole - atropa belladonna - basic cupric carbonate - bryonia alba root - matricaria chamomilla whole - calcium sulfide - citric acid monohydrate - echinacea angustifolia - ferric phosphate - phytolacca americana root - rancid beef - sodium pyruvate - pork liver - rancid beef - sus scrofa pituitary gland -
Active ingredients: Arnica montana — 3 [hp_X]/30mLEchinacea angustifolia whole — 4 [hp_X]/30mLRancid beef — 30 [hp_X]/30mLBasic cupric carbonate — 4 [hp_X]/30mLMatricaria chamomilla whole — 2 [hp_X]/30mLAconitum napellus whole — 6 [hp_X]/30mLApis mellifera — 6 [hp_X]/30mLAtropa belladonna — 6 [hp_X]/30mLBryonia alba root — 6 [hp_X]/30mLCitric acid monohydrate — 3 [hp_X]/30mLFerric phosphate — 12 [hp_X]/30mLCalcium sulfide — 6 [hp_X]/30mLSodium pyruvate — 3 [hp_X]/30mLPhytolacca americana root — 6 [hp_X]/30mLPork liver — 6 [hp_X]/30mLSus scrofa pituitary gland — 200 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 24, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Allergens (Chemical structure)Bee Venoms (Chemical structure)Calcium Chelating Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Decreased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Iron (Chemical structure)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 17089-464_af5aec5c-a562-6516-e053-2a95a90a3be9SPL ID af5aec5c-a562-6516-e053-2a95a90a3be9SPL set ID af5a9c74-e1c7-6574-e053-2995a90a3d10UNII O80TY208ZW, VB06AV5US8, 29SUH5R3HU, GIK928GH0Y, G0R4UBI2ZZ, U0NQ8555JD, 7S82P3R43Z, WQZ3G9PF0H, T7J046YI2B, 2968PHW8QP, N6BAA189V1, 1MBW07J51Q, POD38AIF08, 11E6VI8VEG, 6EC706HI7F, L0PFEMQ1DT
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent; Parenteral Iron Replacement; Phosphate Binder; Standardized Insect Venom 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

N417089046418 followed by a unit qualifier and the quantity

Package 17089-0464-18. 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 Sep 15, 2020.

Indications (excerpt from the label)

DIRECTIONS Take 15 minutes before meals

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)