Home NDC 85248-192 BeamBalm ANTIFUNGAL FOOT SOAKING PACK
Product NDC 85248-192
11-digit product format 852480192
Labeler code 85248
Product ID 85248-192_558a7bc0-2bc4-817f-e063-6294a90ae19f
Type HUMAN OTC DRUG
Nonproprietary name ZINC UNDECYLENATE 5% ANTIFUNGAL FOOT SOAKING PACK
Dosage form POWDER
Route TOPICAL
Labeler Jiangxi Yudexi Pharmaceutical Co., LTD
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-22
Substance ZINC UNDECYLENATE
Active strength 5 g/100g
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 BeamBalm ANTIFUNGAL FOOT SOAKING PACK
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC UNDECYLENATE 5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 388VZ25DUR Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85248-192-01 BeamBalm ANTIFUNGAL FOOT SOAKING PACK 5 g in 1 BAG POWDER 5 1 85248-192-01 BeamBalm ANTIFUNGAL FOOT SOAKING PACK 20 in 1 BAG POWDER 20 1
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 85248-192-01 85248019201 20 BAG in 1 BAG (85248-192-01) / 5 g in 1 BAG 20 bag 2026-04-22 No No Current