Guna-Cough NDC 17089-453

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-453Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0453Add 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
17089-453-24	17089045324	1 BOTTLE in 1 BOX (17089-453-24) / 150 mL in 1 BOTTLEMarketed from Apr 9, 2018

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-Cough
Generic name (nonproprietary): althaea officinalis leaf - antimony potassium tartrate - bryonia alba root - cetraria islandica subsp. islandica - cochineal - copper - drosera rotundifolia - echinacea angustifolia - garden thyme - lobaria pulmonaria - plantago major -
Active ingredients: Althaea officinalis leaf — 1 [hp_X]/150mLAntimony potassium tartrate — 8 [hp_X]/150mLBryonia alba root — 6 [hp_X]/150mLCetraria islandica subsp. Islandica — 4 [hp_X]/150mLCochineal — 6 [hp_X]/150mLCopper — 8 [hp_X]/150mLDrosera rotundifolia — 1 [hp_X]/150mLEchinacea angustifolia — 1 [hp_X]/150mLPlantago major — 1 [hp_X]/150mLLobaria pulmonaria — 4 [hp_X]/150mLThyme — 1 [hp_X]/150mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 27, 2010
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 17089-453_b2576e8c-11d8-1d15-e053-2a95a90a72b1SPL ID b2576e8c-11d8-1d15-e053-2a95a90a72b1SPL set ID 40e9509c-5cc2-4077-ab89-34bec9015f42UNII E2QQV92338, DL6OZ476V3, T7J046YI2B, BJ7YPN79A1, TZ8Z31B35M, 789U1901C5, QR44N9XPJQ, VB06AV5US8, W2469WNO6U, D1YM0P5Z2T, CW657OBU4NUPC 0317089453246
Pharmacologic class: Copper-containing Intrauterine Device; Non-Standardized Food 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

N417089045324 followed by a unit qualifier and the quantity

Package 17089-0453-24. 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 Oct 23, 2020.

Indications (excerpt from the label)

Directions: use enclosed cup for dosing.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)