Gillette Clear Arctic Ice

Dosage form: gel
Ingredients: Aluminum Zirconium Octachlorohydrex Gly 0.16g in 1g
Labeler: Procter & Gamble Manufacturing Company
NDC Code: 37000-265

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.

Gillette®
CLEAR
GEL
ARCTIC ICE

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, trisiloxane, calcium chloride, PEG/PPG-18/18 dimethicone, fragrance

Questions?

1-800-445-5388

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

PRINCIPAL DISPLAY PANEL - 85 g Canister Label

Gillette®
CLEAR
GEL

ARCTIC ICE

Aluminum zirconium octachlorohydrex Gly
Anti-Perspirant/Deodorant

98654914

NET WT. 3.0 OZ (85 g)

GILLETTE CLEAR   ARCTIC ICE
aluminum zirconium octachlorohydrex gly gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-265
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum Zirconium Octachlorohydrex Gly (Aluminum Cation) Aluminum Zirconium Octachlorohydrex Gly0.16 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
water 
cyclomethicone 5 
propylene glycol 
dimethicone 
trisiloxane 
calcium chloride 
Packaging
#Item CodePackage Description
1NDC:37000-265-40113 g in 1 CANISTER
2NDC:37000-265-3085 g in 1 CANISTER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35005/01/2008
Labeler - Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIOperations
The Procter & Gamble Manufacturing Company017745779MANUFACTURE(37000-265)

Revised: 10/2011
 
Procter & Gamble Manufacturing Company

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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