GILLETTE ODOR SHIELD FRESH RESPONSE - aluminum zirconium trichlorohydrex gly stick
Procter & Gamble Manufacturing Company

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Gillette®
ODOR SHIELD
FRESH RESPONSE

Drug Facts

Active ingredient

Aluminum zirconium trichlorohydrex Gly 18% (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

cyclopentasiloxane, stearyl alcohol, C12-15 alkyl benzoate, PPG-14 butyl ether, hydrogenated castor oil, petrolatum, talc, phenyl trimethicone, cyclodextrin, fragrance, mineral oil, behenyl alcohol

Questions?

1-800-445-5388

www.gillette.com

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

PRINCIPAL DISPLAY PANEL - 73 g Canister Label

NEW!

Gillette®
ODOR SHIELD

FRESH RESPONSE

Aluminum zirconium trichlorohydrex Gly
Anti-Perspirant/Deodorant

NET WT. 2.6 OZ (73 g)

Principal Display Panel - 73 g Canister Label

GILLETTE ODOR SHIELD FRESH RESPONSE
aluminum zirconium trichlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	NDC Product Code (Source)	37000-774
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Aluminum Zirconium Trichlorohydrex Gly (Aluminum Cation)	Aluminum Zirconium Trichlorohydrex Gly	0.18 g in 1 g

Inactive Ingredients
Ingredient Name	Strength
cyclomethicone 5
stearyl alcohol
Alkyl (C12-15) Benzoate
PPG-14 butyl ether
hydrogenated castor oil
petrolatum
talc
phenyl trimethicone
mineral oil
docosanol

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	NDC	Package Description	Multilevel Packaging
1	37000-774-73	73 g In 1 CANISTER	None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part350	01/01/2010

Labeler - Procter & Gamble Manufacturing Company (004238200)

Revised: 01/2011Procter & Gamble Manufacturing Company