Home NDC 75543-309 Antibacterial Hand Wipe
Product NDC 75543-309
11-digit product format 755430309
Labeler code 75543
Product ID 75543-309_49279dff-61a6-878f-e063-6394a90a7f12
Type HUMAN OTC DRUG
Nonproprietary name Antibacterial Hand Wipe
Dosage form CLOTH
Route TOPICAL
Labeler Fujian Yifa Healthcare Products Co., Ltd.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-26
Substance BENZALKONIUM CHLORIDE
Active strength .2 g/401
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 Antibacterial Hand Wipe
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .2 g/401
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 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 75543-309-00 Antibacterial Hand Wipe 40 in 1 PACKAGE CLOTH 40 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 100 of 114 · 2,277 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 75543-309-00 75543030900 40 CLOTH in 1 PACKAGE (75543-309-00) 40 cloth 2026-01-26 No No Current