Home NDC 11523-7155 Lotrimin Ultra Jock Itch
Product NDC 11523-7155
11-digit product format 115237155
Labeler code 11523
Product ID 11523-7155_47e50ab6-503b-0fe0-e054-00144ff8d46c
Type HUMAN OTC DRUG
Nonproprietary name Butenafine Hydrochloride
Dosage form CREAM
Route TOPICAL
Labeler Bayer HealthCare LLC.
Application NDA021307
Marketing category NDA
Marketing start 1993-09-23
Marketing end 0000-00-00
Substance BUTENAFINE HYDROCHLORIDE
Active strength 10 mg/g
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record NDC auxiliary status# Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table Dataset Scope Product NDC Package NDC Code Status Reporting period Source date excluded product product 11523-7155 D Discontinued by firm 2026-07-31 excluded package package 11523-7155 11523-7155-1 D Discontinued by firm 2026-07-31 excluded package package 11523-7155 11523-7155-2 D Discontinued by firm 2026-07-31
Orange Book products# Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N021307-001 LOTRIMIN ULTRA BUTENAFINE HYDROCHLORIDE 1% CREAM / TOPICAL RLD, RS 2001-12-07
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings For external use only Do not use on nails or scalp in or near the mouth or the eyes for vaginal yeast infections When using this product do not get into the eyes. If eye contact occurs, rinse thoroughly with water. Stop use and ask a doctor if too much irritation occurs or irritation gets worse Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Butenafine Hydrochloride ACTIVE INGREDIENT R8XA2029ZI LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 Butenafine ACTIVE MOIETY 91Y494NL0X LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 benzyl alcohol INACTIVE INGREDIENT LKG8494WBH LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 ceteth-23 INACTIVE INGREDIENT 495CTZ441V LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 cetyl alcohol INACTIVE INGREDIENT 936JST6JCN LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 diethanolamine INACTIVE INGREDIENT AZE05TDV2V LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 glycerin INACTIVE INGREDIENT PDC6A3C0OX LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 petrolatum INACTIVE INGREDIENT 4T6H12BN9U LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 propylene glycol dicaprylate INACTIVE INGREDIENT 581437HWX2 LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 sodium benzoate INACTIVE INGREDIENT OJ245FE5EU LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 stearic acid INACTIVE INGREDIENT 4ELV7Z65AP LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2 water INACTIVE INGREDIENT 059QF0KO0R LOTRIMIN ULTRA JOCK ITCH ANTIFUNGAL (BUTENAFINE HYDROCHLORIDE) CREAM [MSD CONSUMER CARE, INC.] 2