PURELL HEALTHY SP 0.5pct BAK Antimicrobial Foam

Product NDC
21749-684
11-digit product format
217490684
Labeler code
21749
Product ID
21749-684_292bf620-5cd2-388d-e063-6394a90a307c
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
2021-12-15
Substance
BENZALKONIUM CHLORIDE
Active strength
.005 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
PURELL HEALTHY SP 0.5pct BAK Antimicrobial Foam
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE.005 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF5UM2KM3W7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-684-40PURELL HEALTHY SP 0.5pct BAK Antimicrobial Foam1200 mL in 1 PACKAGELIQUID12003
21749-684-67PURELL HEALTHY SP 0.5pct BAK Antimicrobial Foam2000 mL in 1 PACKAGELIQUID20003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-684PURELL HEALTHY SP 0.5PCT BAK ANTIMICROBIAL FOAM (BENZALKONIUM CHLORIDE) LIQUID [GOJO INDUSTRIES, INC.]3Current NDC, Legacy NDC, 2 package rows20241215_97b7d732-3b33-4c60-b6d9-0f1d28dda4bf.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21749-684-40217490684401200 mL in 1 PACKAGE (21749-684-40) 1200 ml2021-12-150000-00-00NoNoCurrent
21749-684-67217490684672000 mL in 1 PACKAGE (21749-684-67) 2000 ml2021-12-150000-00-00NoNoCurrent