Dove Clinical Protection Cool Essentials 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 Clinical Protection Cool Essentials Antiperspirant and Deodorant
Generic name: ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Manufacturer: Conopco Inc. d/b/a Unilever
Product type: HUMAN OTC DRUG
SPL set ID: de02841f-5eb9-4d45-9243-5dfc50784a68
SPL ID: 253bd5bd-b639-af53-e063-6394a90aadbc
Version: 5
Effective date: 2024-10-24
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:15:35

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 Clinical Protection Cool Essentials 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	64942-1441-7	openfda.package_ndc
ndc	package	64942-1441-8	openfda.package_ndc
ndc	package	64942-1441-1	openfda.package_ndc
ndc	package	64942-1441-2	openfda.package_ndc
ndc	package	64942-1441-6	openfda.package_ndc
ndc	package	64942-1441-3	openfda.package_ndc
ndc	package	64942-1441-4	openfda.package_ndc
ndc	package	64942-1441-5	openfda.package_ndc
ndc	product	64942-1441	openfda.product_ndc
ndc11	package	64942144101	derived:openfda.package_ndc
ndc11	package	64942144108	derived:openfda.package_ndc
ndc11	package	64942144102	derived:openfda.package_ndc
ndc11	package	64942144105	derived:openfda.package_ndc
ndc11	package	64942144106	derived:openfda.package_ndc
ndc11	package	64942144103	derived:openfda.package_ndc
ndc11	package	64942144107	derived:openfda.package_ndc
ndc11	package	64942144104	derived:openfda.package_ndc
spl id		253bd5bd-b639-af53-e063-6394a90aadbc	id
spl set id		de02841f-5eb9-4d45-9243-5dfc50784a68	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.