Gillette Supreme Protection Cool Wave Clear

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: Gillette Supreme Protection Cool Wave Clear
Generic name: ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: 3f6a034e-bf9c-134d-e063-6394a90a4700
SPL ID: 3f6a031f-03fc-da7e-e063-6294a90a8457
Version: 1
Effective date: 2025-09-22
Source export date: 2026-11-06
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/7dfa569f2d8f065241260fd9a4886d0ef0a3120fd6ee31d6d07c234e689e8c91/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:21:46

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M019	openfda.application_number
brand name		Gillette Supreme Protection Cool Wave Clear	openfda.brand_name
generic name		ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY	openfda.generic_name
manufacturer name		The Procter & Gamble Manufacturing Company	openfda.manufacturer_name
ndc	package	84126-181-10	openfda.package_ndc
ndc	package	84126-181-01	openfda.package_ndc
ndc	product	84126-181	openfda.product_ndc
ndc11	package	84126018110	derived:openfda.package_ndc
ndc11	package	84126018101	derived:openfda.package_ndc
spl id		3f6a031f-03fc-da7e-e063-6294a90a8457	id
spl set id		3f6a034e-bf9c-134d-e063-6394a90a4700	set_id
unii		P9D3YP29MY	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.