GOJO E2 Foam Handwash with BAK

Product NDC
21749-112
11-digit product format
217490112
Labeler code
21749
Product ID
21749-112_28640b27-2a60-0c58-e063-6394a90a4df2
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
2019-03-01
Substance
BENZALKONIUM CHLORIDE
Active strength
.0013 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
GOJO E2 Foam Handwash with BAK
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE.0013 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF5UM2KM3W7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-112-20GOJO E2 Foam Handwash with BAK2000 mL in 1 PACKAGELIQUID20002
21749-112-89GOJO E2 Foam Handwash with BAK1200 mL in 1 PACKAGELIQUID12002
21749-112-90GOJO E2 Foam Handwash with BAK1250 mL in 1 PACKAGELIQUID12502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-112GOJO E2 FOAM HANDWASH WITH BAK (BENZALKONIUM CHLORIDE) LIQUID [GOJO INDUSTRIES, INC.]2Current NDC, Legacy NDC, 3 package rows20241206_f18732bd-65c7-4e11-b364-054b7e742505.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21749-112-20217490112202000 mL in 1 PACKAGE (21749-112-20) 2000 ml2019-03-010000-00-00NoNoCurrent
21749-112-89217490112891200 mL in 1 PACKAGE (21749-112-89) 1200 ml2019-03-010000-00-00NoNoCurrent
21749-112-90217490112901250 mL in 1 PACKAGE (21749-112-90) 1250 ml2019-03-010000-00-00NoNoCurrent