FOAMING HAND ANTIBACTERIAL

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: FOAMING HAND ANTIBACTERIAL
Generic name: CHLOROXYLENOL
Manufacturer: Draco Hygienic Products Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 15256355-29ef-9b24-e063-6294a90a907d
SPL ID: 23f9338f-4538-64ed-e063-6394a90ada99
Version: 2
Effective date: 2024-10-08
Source export date: 2026-11-06
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/2026-11-06/8ec9b1418c25a8bb472a36e6bc0b2cbabb210d48d5dd734197e022d21529ed58/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 09:18:51

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		FOAMING HAND ANTIBACTERIAL	openfda.brand_name
generic name		CHLOROXYLENOL	openfda.generic_name
manufacturer name		Draco Hygienic Products Inc.	openfda.manufacturer_name
ndc	package	83019-103-11	openfda.package_ndc
ndc	product	83019-103	openfda.product_ndc
ndc11	package	83019010311	derived:openfda.package_ndc
rxcui		2002728	openfda.rxcui
spl id		23f9338f-4538-64ed-e063-6394a90ada99	id
spl set id		15256355-29ef-9b24-e063-6294a90a907d	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 AVOID CONTACT WITH EYES. IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN. STOP USE THIS PRODUCT AND ASK A DOCTOR IF CONDITIONS WORSEN OR IRRITATION PERSISTS. IRRITATION OR REDNESS DEVELOPS AND PERSISTED FOR MORE THAN 72 HOURS.

Reported adverse events (FAERS/openFDA)#

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