Home NDC 87786-038 XBOFPEN MULTI-PURPOSE TREATMENT
Product NDC 87786-038
11-digit product format 877860038
Labeler code 87786
Product ID 87786-038_58c2f50c-9c9f-4989-e063-6394a90abb21
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate 1% MULTI-PURPOSE TREATMENT
Dosage form LIQUID
Route TOPICAL
Labeler Wenzhou Yuyuan Pharmaceutical Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-11
Substance TOLNAFTATE
Active strength 1 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base XBOFPEN MULTI-PURPOSE TREATMENT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 06KB629TKV Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313423 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 8 of 49 · 973 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87786-038-01 87786003801 30 mL in 1 BOTTLE (87786-038-01) 30 ml 2026-08-11 No No Current