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Drug Facts
Antiperspirant-deodorant Roll-on Liquid
FDA Label NDC 49527-076
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Clinique Laboratories Llc for the product Antiperspirant-deodorant Roll-on (NDC 49527-076). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, active ingredient, purpose, use, warnings, otc - do not use, otc - stop use, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
Principal Display Panel (75 ml Bottle Label)
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