Purell Antimicrobial Foam

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Purell Antimicrobial Foam
Generic name: CHLORHEXIDINE GLUCONATE 2% SOLUTION
Manufacturer: GOJO Industries, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 6c7e63c2-428b-2be2-e053-2a91aa0a6af3
SPL ID: 29cc1350-3ead-511d-e063-6394a90aa388
Version: 4
Effective date: 2024-12-21
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:39

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	NDA	019422	derived:openfda.application_number
application number		NDA019422	openfda.application_number
brand name		Purell Antimicrobial Foam	openfda.brand_name
generic name		CHLORHEXIDINE GLUCONATE 2% SOLUTION	openfda.generic_name
manufacturer name		GOJO Industries, Inc.	openfda.manufacturer_name
ndc	package	21749-225-64	openfda.package_ndc
ndc	package	21749-225-58	openfda.package_ndc
ndc	package	21749-225-57	openfda.package_ndc
ndc	package	21749-225-68	openfda.package_ndc
ndc	package	21749-225-56	openfda.package_ndc
ndc	product	21749-225	openfda.product_ndc
ndc11	package	21749022558	derived:openfda.package_ndc
ndc11	package	21749022568	derived:openfda.package_ndc
ndc11	package	21749022556	derived:openfda.package_ndc
ndc11	package	21749022557	derived:openfda.package_ndc
ndc11	package	21749022564	derived:openfda.package_ndc
rxcui		1245230	openfda.rxcui
spl id		29cc1350-3ead-511d-e063-6394a90aa388	id
spl set id		6c7e63c2-428b-2be2-e053-2a91aa0a6af3	set_id
unii		MOR84MUD8E	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Allergy alert: This product may cause severe allergic reaction. Symptoms may include: wheezing/difficulty breathing shock facial swelling hives rash If an allergic reaction occurs, stop use and seek medical help right away.

Reported adverse events (FAERS/openFDA)#

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