NDC 72657-166

NDC codes

FDA NDC Directory

Product NDC (as listed)72657-166Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72657-0166Add 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
72657-166-72	72657016672	1 BOTTLE in 1 CARTON (72657-166-72) / 72 SPRAY, METERED in 1 BOTTLEMarketed from Jun 30, 2026

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): Childrens Fluticasone Propionate ALLERGY RELIEFSuffix: ALLERGY RELIEF
Generic name (nonproprietary): fluticasone propionate
Active ingredients: Fluticasone propionate — 50 ug/1
Dosage form: Spray, Metered
Route: Nasal
Labeler: GLENMARK THERAPEUTICS INC., USA
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218742
Marketing start: Jun 30, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 72657-166_9aaa30cf-1e3b-4382-91dc-568067a4b0acSPL ID 9aaa30cf-1e3b-4382-91dc-568067a4b0acSPL set ID 9aaa30cf-1e3b-4382-91dc-568067a4b0acRxCUI 1797907UNII O2GMZ0LF5WUPC 0372657166720
Pharmacologic class: Corticosteroid

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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472657016672 followed by a unit qualifier and the quantity

Package 72657-0166-72. 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 30, 2026.

Indications (excerpt from the label)

Uses Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • itchy nose • runny nose • itchy, watery eyes • sneezing

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 218742

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 218742
Product	Strength	Form · route	Labeler	Product NDC
Fluticasone Propionate ALLERGY RELIEFfluticasone propionate	Fluticasone propionate 50 ug/1	Spray, MeteredNasal	GLENMARK THERAPEUTICS INC., USA	72657-159
Fluticasone Propionate ALLERGY RELIEFfluticasone propionate	Fluticasone propionate 50 ug/1	Spray, MeteredNasal	YYBA CORP	73581-530

Childrens Fluticasone Propionate ALLERGY RELIEF NDC 72657-166