PURELL HEALTHY SP BAK E2 Antimicrobial Foam Sp

Product NDC
21749-113
11-digit product format
217490113
Labeler code
21749
Product ID
21749-113_2864054a-7e5d-2024-e063-6394a90a3d22
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
2022-01-01
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
PURELL HEALTHY SP BAK E2 Antimicrobial Foam Sp
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
21749-113-40PURELL HEALTHY SP BAK E2 Antimicrobial Foam Sp2000 mL in 1 PACKAGELIQUID20003
21749-113-42PURELL HEALTHY SP BAK E2 Antimicrobial Foam Sp1250 mL in 1 PACKAGELIQUID12503
21749-113-67PURELL HEALTHY SP BAK E2 Antimicrobial Foam Sp1200 mL in 1 PACKAGELIQUID12003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-113PURELL HEALTHY SP BAK E2 ANTIMICROBIAL FOAM SP (BENZALKONIUM CHLORIDE) LIQUID [GOJO INDUSTRIES, INC.]3Current NDC, Legacy NDC, 3 package rows20241206_4ea02d8a-cb03-4e9e-b63d-72b83fa816f8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21749-113-40217490113402000 mL in 1 PACKAGE (21749-113-40) 2000 ml2022-01-010000-00-00NoNoCurrent
21749-113-42217490113421250 mL in 1 PACKAGE (21749-113-42) 1250 ml2022-01-010000-00-00NoNoCurrent
21749-113-67217490113671200 mL in 1 PACKAGE (21749-113-67) 1200 ml2022-01-010000-00-00NoNoCurrent