Home NDC 71912-521 ADVANTAGE CHEMICAL Premium Antibacterial Foaming Hand So ap
Product NDC 71912-521
11-digit product format 719120521
Labeler code 71912
Product ID 71912-521_29a4e82a-213a-3542-e063-6394a90a96a5
Type HUMAN OTC DRUG
Nonproprietary name CHLOROXYLENOL
Dosage form LIQUID
Route TOPICAL
Labeler Advantage Chemical, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-04-15
Substance CHLOROXYLENOL
Active strength .005 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 ADVANTAGE CHEMICAL Premium Antibacterial Foaming Hand So ap
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CHLOROXYLENOL .005 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0F32U78V2Q Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71912-521-42 ADVANTAGE CHEMICAL Premium Antibacterial Foaming Hand So ap 1250 mL in 1 BOTTLE LIQUID 1250 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71912-521 ADVANTAGE CHEMICAL PREMIUM ANTIBACTERIAL FOAMING HAND SO AP (CHLOROXYLENOL) LIQUID [ADVANTAGE CHEMICAL, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20241222_69dbc2ac-c308-4604-bc64-bcfa43ed3ad0.zip
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71912-521-42 71912052142 1250 mL in 1 BOTTLE (71912-521-42) 1250 ml 2015-04-15 0000-00-00 No No Current