GILLETTE ENDURANCE WILD RAIN CLEAR- aluminum zirconium octachlorohydrex gly gel 
The Procter & Gamble Manufacturing Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Gillette Endurance Wild Rain Clear Gel

Drug Facts

Active ingredient

Aluminum zirconium octachlorohydrex Gly 16% (anhydrous)

Purpose

Antiperspirant

Use

  • reduces underarm wetness

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.

Directions

  • apply to underarms only

Inactive ingredients

water,alcohol denat., cyclopentasiloxane, propylene glycol, dimethicone, calcium chloride, PEG/PPG-18/18 dimethicone, fragrance

Questions?

1-800-445-5388

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 107 g Canister

Gillette ®

ENDURANCE

ELIMINATES ODOR

AT THE SOURCE

WILD RAIN
CLEAR GEL

ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY


ANTI-PERSPIRANT/DEODORANT

NET WT. 3.8 OZ (107 g)Gillette

GILLETTE ENDURANCE WILD RAIN CLEAR 
aluminum zirconium octachlorohydrex gly gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-200
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY) (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY - UNII:P9D3YP29MY) ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY16 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-200-10107 g in 1 CANISTER; Type 0: Not a Combination Product06/20/201708/26/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35006/20/201708/26/2019
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 12/2017
Document Id: 5f49e65c-dc7c-35f0-e053-2991aa0ae99f
Set id: 5151bb4f-10a9-584f-e054-00144ff88e88
Version: 2
Effective Time: 20171201
 
The Procter & Gamble Manufacturing Company