Dove Clinical Protection Soothing Chamomile 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 Soothing Chamomile Antiperspirant and Deodorant
Generic name: ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Manufacturer: Conopco Inc. d/b/a Unilever
Product type: HUMAN OTC DRUG
SPL set ID: 1647d392-cf8a-46b1-9d45-656ac79b223b
SPL ID: 253ba50c-6c5a-468c-e063-6394a90a661a
Version: 7
Effective date: 2024-10-24
Source export date: 2026-10-12
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:44:04

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 number		M019	openfda.application_number
brand name		Dove Clinical Protection Soothing Chamomile 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	64942-1222-6	openfda.package_ndc
ndc	package	64942-1222-5	openfda.package_ndc
ndc	package	64942-1222-2	openfda.package_ndc
ndc	package	64942-1222-4	openfda.package_ndc
ndc	package	64942-1222-3	openfda.package_ndc
ndc	package	64942-1222-1	openfda.package_ndc
ndc	product	64942-1222	openfda.product_ndc
ndc11	package	64942122205	derived:openfda.package_ndc
ndc11	package	64942122204	derived:openfda.package_ndc
ndc11	package	64942122202	derived:openfda.package_ndc
ndc11	package	64942122206	derived:openfda.package_ndc
ndc11	package	64942122201	derived:openfda.package_ndc
ndc11	package	64942122203	derived:openfda.package_ndc
spl id		253ba50c-6c5a-468c-e063-6394a90a661a	id
spl set id		1647d392-cf8a-46b1-9d45-656ac79b223b	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.