Gillette Clinical Protection Cool Wave Clear

Product NDC
69423-584
11-digit product format
694230584
Labeler code
69423
Product ID
69423-584_2fb4c211-96a7-4a65-e063-6394a90a0b09
Type
HUMAN OTC DRUG
Nonproprietary name
Aluminum Zirconium Octachlorohydrex Gly
Dosage form
GEL
Route
TOPICAL
Labeler
The Procter & Gamble Manufacturing Company
Application
M019
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-01-01
Substance
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
Active strength
20 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
P9D3YP29MYALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY174514-58-0ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69423-584-45694230584451 CANISTER in 1 CARTON (69423-584-45) / 45 g in 1 CANISTER1 canister2021-01-01NoNoHistorical
69423-584-73694230584731 CANISTER in 1 CARTON (69423-584-73) / 73 g in 1 CANISTER1 canister2021-01-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Gillette ® Clinical Protection Cool Wave Clear GelThe Procter & Gamble Manufacturing Company2025-03-06HUMAN OTC DRUG LABEL3