FDA Label for Antiperspirant-deodorant Roll-on
View Indications, Usage & Precautions
Antiperspirant-deodorant Roll-on Product Label
The following document was submitted to the FDA by the labeler of this product Clinique Laboratories Llc. 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.
Other
Drug Facts
Active Ingredient
Aluminum chlorohydrate 18.20%
Purpose
Antiperspirant
Use
Reduces underarm wetness
Warnings
For external use only
Otc - Do Not Use
Do not use on broken skin
Otc - Stop Use
Stop use if irritation occurs
Otc - Ask Doctor
Ask a doctor before use if you have kidney disease
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\aqua\eau • ceteth-2 • ppg-11 stearyl ether • steareth-20 • myristalkonium chloride • quaternium-14 • sorbic acid • trisodium edta [iln37802]
Principal Display Panel - 75 Ml Bottle Label
C
CLINIQUE
antiperspirant-
deodorant
roll-on
ALUMINUM CHLOROHYDRATE
2.5 FL.OZ.LIQ./75 ml e
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