GILLETTE CLINICAL COOL WAVE 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 ® Clinical

Clear Cool Wave

Drug Facts

Active ingredient

Aluminum zirconium octachlorohydrex Gly 20% (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
  • apply 3 - 4 clicks of product to underarms at bedtime
  • rub in until clear

Inactive ingredients

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

Questions?

1-800-445-5388

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

PRINCIPAL DISPLAY PANEL - 45 g Canister Carton

Gillette®

CLINICAL

PROTECTION

48 HR

EXTREME

SWEAT PROTECTION

COOL WAVE
CLEAR GEL

ALUMINUM ZIRCONIUM

OCTACHLOROHYDREX GLY
ANTI-PERSPIRANT/DEODORANT

NET WT. 1.6 OZ. (45 g)

Gill

GILLETTE CLINICAL  COOL WAVE CLEAR
aluminum zirconium octachlorohydrex gly gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-157
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 GLY20 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
WATER (UNII: 059QF0KO0R)  
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:69423-157-451 in 1 CARTON02/02/201606/15/2023
145 g in 1 CANISTER; Type 0: Not a Combination Product
2NDC:69423-157-731 in 1 CARTON02/02/201606/15/2023
273 g in 1 CANISTER; Type 0: Not a Combination Product
3NDC:69423-157-141 in 1 CARTON02/02/201608/31/2018
314 g in 1 CANISTER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35002/02/201606/15/2023
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 1/2022
Document Id: d6957d5e-ea9c-d1f4-e053-2995a90a5b12
Set id: 41ff7329-e503-1b54-e054-00144ff8d46c
Version: 4
Effective Time: 20220127
 
The Procter & Gamble Manufacturing Company