Clotrimazole Topical Solution USP, 1% NDC 72162-2178

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2178Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2178Add 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
72162-2178-3	72162217803	1 BOTTLE in 1 CARTON (72162-2178-3) / 30 mL in 1 BOTTLEMarketed from Jul 25, 2019

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): Clotrimazole Topical Solution USP, 1%
Generic name (nonproprietary): clotrimazole topical solution usp, 1%
Active ingredients: Clotrimazole — 10 mg/mL
Dosage form: Solution
Route: Topical
Labeler: Bryant Ranch Prepack
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212281
Marketing start: Jul 25, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Azoles (Chemical structure)
Identifiers: Product ID 72162-2178_8acb584d-a5f9-4956-8b29-b20005b1766eSPL ID 8acb584d-a5f9-4956-8b29-b20005b1766eSPL set ID 6a50410d-ef84-4b60-9bec-cf1d1166e461RxCUI 309370UNII G07GZ97H65
Pharmacologic class: Azole Antifungal

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

NDC on a medical claim

N472162217803 followed by a unit qualifier and the quantity

Package 72162-2178-03. 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 Mar 19, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Prescription clotrimazole topical solution product is indicated for the topical treatment of candidiasis due to Candida albicans and tinea versicolor due to Malassezia furfur . This formulation is also available as a nonprescription product which is indicated for the topical treatment of the following dermal infections: tinea pedis, tinea cruris, and tinea corporis due to Trichophyton rubrum, Trichophyton mentagrophytes , Epidermophyton fluoccosum , and Microsporum canis .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 212281

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

FDA NDC Directory listings under ANDA 212281
Product	Strength	Form · route	Labeler	Product NDC
Clotrimazole Topical Solution USP, 1%	Clotrimazole 10 mg/mL	SolutionTopical	TruPharma LLC	52817-800