Dove Men Clinical Protection Clean Comfort Antiperspirant and Deodorant

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: Dove Men Clinical Protection Clean Comfort Antiperspirant and Deodorant
Generic name: ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Manufacturer: Conopco Inc. d/b/a Unilever
Product type: HUMAN OTC DRUG
SPL set ID: 9dd9674e-34eb-43a5-8a01-3f3703c16fb4
SPL ID: 253b7c3a-1204-70cc-e063-6394a90a1241
Version: 10
Effective date: 2024-10-24
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:24:03

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M019	openfda.application_number
brand name		Dove Men Clinical Protection Clean Comfort Antiperspirant and Deodorant	openfda.brand_name
generic name		ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	openfda.generic_name
manufacturer name		Conopco Inc. d/b/a Unilever	openfda.manufacturer_name
ndc	package	64942-1163-8	openfda.package_ndc
ndc	package	64942-1163-6	openfda.package_ndc
ndc	package	64942-1163-2	openfda.package_ndc
ndc	package	64942-1163-7	openfda.package_ndc
ndc	package	64942-1163-5	openfda.package_ndc
ndc	package	64942-1163-4	openfda.package_ndc
ndc	package	64942-1163-3	openfda.package_ndc
ndc	package	64942-1163-1	openfda.package_ndc
ndc	product	64942-1163	openfda.product_ndc
ndc11	package	64942116305	derived:openfda.package_ndc
ndc11	package	64942116301	derived:openfda.package_ndc
ndc11	package	64942116306	derived:openfda.package_ndc
ndc11	package	64942116307	derived:openfda.package_ndc
ndc11	package	64942116303	derived:openfda.package_ndc
ndc11	package	64942116308	derived:openfda.package_ndc
ndc11	package	64942116302	derived:openfda.package_ndc
ndc11	package	64942116304	derived:openfda.package_ndc
spl id		253b7c3a-1204-70cc-e063-6394a90a1241	id
spl set id		9dd9674e-34eb-43a5-8a01-3f3703c16fb4	set_id
unii		8O386558JE	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 Do not use on broken skin Ask a doctor before use if you have kidney disease Stop use if rash or irritation occurs 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.