FDA.reportPublic FDA data

GOJO Mild Antibacterial Foam Hand Sp

Manufacturer
GOJO Industries, Inc.
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:49:33

Label at a glance#

ProductGOJO Mild Antibacterial Foam Hand Sp
Active ingredientBENZALKONIUM CHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct LabelProduct LabelProduct Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-051-53GOJO Mild Antibacterial Foam Hand Sp535 mL in 1 PACKAGELIQUID5355
21749-051-89GOJO Mild Antibacterial Foam Hand Sp1200 mL in 1 PACKAGELIQUID12005
21749-051-90GOJO Mild Antibacterial Foam Hand Sp1250 mL in 1 PACKAGELIQUID12505
21749-051-97GOJO Mild Antibacterial Foam Hand Sp700 mL in 1 PACKAGELIQUID7005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-051GOJO MILD ANTIBACTERIAL FOAM HAND SP (BENZALKONIUM CHLORIDE) LIQUID [GOJO INDUSTRIES, INC.]54 package rows20250101_11753bc4-a873-41d7-9a1b-e4470e76d0a0.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-05121749-051-53, 21749-051-97, 21749-051-89, 21749-051-90

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PEG-80 SORBITAN LAURATE239B50Y732IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
POLYQUATERNIUM-10 (10000 MPA.S AT 2%)PI1STR9QYHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2a96b927-af5f-db3c-e063-6394a90a05f811753bc4-a873-41d7-9a1b-e4470e76d0a02024-12-31Exact identifier
spl id: 2a96b927-af5f-db3c-e063-6394a90a05f8
spl set id: 11753bc4-a873-41d7-9a1b-e4470e76d0a0

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.