Secret Fresh Invisible Antiperspirant/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: Secret Fresh Invisible Antiperspirant/Deodorant
Generic name: ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: e78f915f-a3d2-01c2-e053-2995a90ac056
SPL ID: 552b7307-b035-f57f-e063-6294a90ae2e5
Version: 6
Effective date: 2026-06-26
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:17:11

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M019	openfda.application_number
brand name		Secret Fresh Invisible Antiperspirant/Deodorant	openfda.brand_name
generic name		ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY	openfda.generic_name
manufacturer name		The Procter & Gamble Manufacturing Company	openfda.manufacturer_name
ndc	package	69423-631-59	openfda.package_ndc
ndc	package	69423-631-04	openfda.package_ndc
ndc	package	69423-631-14	openfda.package_ndc
ndc	package	69423-631-68	openfda.package_ndc
ndc	package	69423-631-03	openfda.package_ndc
ndc	package	69423-631-02	openfda.package_ndc
ndc	package	69423-631-73	openfda.package_ndc
ndc	package	69423-631-05	openfda.package_ndc
ndc	package	69423-631-45	openfda.package_ndc
ndc	package	69423-631-01	openfda.package_ndc
ndc	product	69423-631	openfda.product_ndc
ndc11	package	69423063145	derived:openfda.package_ndc
ndc11	package	69423063173	derived:openfda.package_ndc
ndc11	package	69423063101	derived:openfda.package_ndc
ndc11	package	69423063105	derived:openfda.package_ndc
ndc11	package	69423063104	derived:openfda.package_ndc
ndc11	package	69423063168	derived:openfda.package_ndc
ndc11	package	69423063103	derived:openfda.package_ndc
ndc11	package	69423063114	derived:openfda.package_ndc
ndc11	package	69423063159	derived:openfda.package_ndc
ndc11	package	69423063102	derived:openfda.package_ndc
spl id		552b7307-b035-f57f-e063-6294a90ae2e5	id
spl set id		e78f915f-a3d2-01c2-e053-2995a90ac056	set_id
unii		94703016SM	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.