FDA Label for Gillette Clear Plus Dri-tech Cool Wave
View Indications, Usage & Precautions
Gillette Clear Plus Dri-tech Cool Wave Product Label
The following document was submitted to the FDA by the labeler of this product The Procter & Gamble Manufacturing Company. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
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Drug Facts
Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.
Active Ingredient
Aluminum zirconium octachlorohydrex Gly 17% (anhydrous)
Purpose
Antiperspirant
Use
reduces underarm wetness
Warnings
For external use only.
Otc - Do Not Use
Do not use on broken skin
Otc - Ask Doctor
Ask a doctor before use if you have kidney disease
Otc - Stop Use
Stop use if rash or irritation occurs
Otc - Keep Out Of Reach Of Children
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
Package Label.Principal Display Panel
Gillette ®
CLEAR + DRI-TECH
COOL WAVE
ANTI-WHITE MARK
ANTIPERSPIRANT PROTECTION
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
ANTI-PERSPIRANT/DEODORANT
NET WT. 3.8 OZ (107 g)
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