Home NDC 21749-687-42 PURELL Healthcare HEALTHY SP 0.5 BAK Antimicrobial Foam
Product NDC 21749-687
Requested package NDC 21749-687-42
11-digit product format 217490687
Labeler code 21749
Product ID 21749-687_292ca55e-76eb-f399-e063-6294a90ab52a
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler GOJO Industries, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-06-15
Substance BENZALKONIUM CHLORIDE
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 PURELL Healthcare HEALTHY SP 0.5 BAK Antimicrobial Foam
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .005 mg/mL
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 21749-687-40 PURELL Healthcare HEALTHY SP 0.5 BAK Antimicrobial Foam 1200 mL in 1 PACKAGE LIQUID 1200 2 21749-687-42 PURELL Healthcare HEALTHY SP 0.5 BAK Antimicrobial Foam 1250 mL in 1 PACKAGE LIQUID 1250 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21749-687 PURELL HEALTHCARE HEALTHY SP 0.5 BAK ANTIMICROBIAL FOAM (BENZALKONIUM CHLORIDE) LIQUID [GOJO INDUSTRIES, INC.] 2 Current NDC, Legacy NDC, 2 package rows 20241215_6f1b969e-77b9-46fd-8642-ffce87a73ecb.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 21749-687-42 21749068742 1250 mL in 1 PACKAGE (21749-687-42) 1250 ml 2019-06-15 0000-00-00 No No Current