GOJO Antimicrobial Foam Handwash with PCMX

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: GOJO Antimicrobial Foam Handwash with PCMX
Generic name: CHLOROXYLENOL
Manufacturer: GOJO Industries, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1f531296-f826-4354-919a-ed356d70e4ba
SPL ID: 285104f0-27c3-e85e-e063-6394a90a2607
Version: 3
Effective date: 2024-12-02
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:24:59

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		GOJO Antimicrobial Foam Handwash with PCMX	openfda.brand_name
generic name		CHLOROXYLENOL	openfda.generic_name
manufacturer name		GOJO Industries, Inc.	openfda.manufacturer_name
ndc	package	21749-521-90	openfda.package_ndc
ndc	package	21749-521-53	openfda.package_ndc
ndc	package	21749-521-97	openfda.package_ndc
ndc	package	21749-521-89	openfda.package_ndc
ndc	product	21749-521	openfda.product_ndc
ndc11	package	21749052153	derived:openfda.package_ndc
ndc11	package	21749052189	derived:openfda.package_ndc
ndc11	package	21749052197	derived:openfda.package_ndc
ndc11	package	21749052190	derived:openfda.package_ndc
rxcui		436367	openfda.rxcui
spl id		285104f0-27c3-e85e-e063-6394a90a2607	id
spl set id		1f531296-f826-4354-919a-ed356d70e4ba	set_id
unii		0F32U78V2Q	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 When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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