Guna Pain Management NDC 17089-465

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-465Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0465Add 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
17089-465-18	17089046518	1 BOTTLE, DROPPER in 1 BOX (17089-465-18) / 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 Pain Management
Generic name (nonproprietary): achillea millefolium whole - bellis perennis whole - matricaria chamomilla whole - toxicodendron pubescens whole - ruta graveolens flowering top - comfrey root - apis mellifera - bryonia alba root - histamine hydrochloride - hypericum perforatum - kalmia latifolia leaf - arnica montana whole - pork liver -
Active ingredients: Bryonia alba root — 6 [hp_X]/30mLHistamine dihydrochloride — 12 [hp_X]/30mLHypericum perforatum — 3 [hp_X]/30mLArnica montana whole — 3 [hp_X]/30mLPork liver — 6 [hp_X]/30mLBellis perennis whole — 2 [hp_X]/30mLMatricaria chamomilla whole — 2 [hp_X]/30mLToxicodendron pubescens leaf — 8 [hp_X]/30mLRuta graveolens flowering top — 4 [hp_X]/30mLKalmia latifolia leaf — 6 [hp_X]/30mLAchillea millefolium whole — 2 [hp_X]/30mLComfrey root — 6 [hp_X]/30mLApis mellifera — 30 [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: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 17089-465_af5b9acf-ede8-0899-e053-2a95a90a1706SPL ID af5b9acf-ede8-0899-e053-2a95a90a1706SPL set ID af5bad63-6d57-2260-e053-2995a90afb7eUNII T7J046YI2B, 3POA0Q644U, XK4IUX8MNB, O80TY208ZW, 6EC706HI7F, 2HU33I03UY, G0R4UBI2ZZ, 6IO182RP7A, N94C2U587S, 79N6542N18, 2FXJ6SW4PK, M9VVZ08EKQ, 7S82P3R43ZUPC 0317089465188
Pharmacologic class: 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

N417089046518 followed by a unit qualifier and the quantity

Package 17089-0465-18. 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)

Take 15 minutes before meals.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)