Home NDC 21749-722 PURELL Antimicrobial Foaming Hand SP with PCMX
Product NDC 21749-722
11-digit product format 217490722
Labeler code 21749
Product ID 21749-722_445cfb03-4528-d117-e063-6294a90afa82
Type HUMAN OTC DRUG
Nonproprietary name Chloroxylenol
Dosage form LIQUID
Route TOPICAL
Labeler GOJO Industries, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-01
Substance CHLOROXYLENOL
Active strength .5 mg/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base PURELL Antimicrobial Foaming Hand SP with PCMX
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CHLOROXYLENOL .5 mg/100mL
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 21749-722-89 PURELL Antimicrobial Foaming Hand SP with PCMX 1200 mL in 1 PACKAGE LIQUID 1200 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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 21749-722-89 21749072289 1200 mL in 1 PACKAGE (21749-722-89) 1200 ml 2025-12-01 No No Current