Otc - Active Ingredient
ACTIVE INGREDIENT:ALUMINUM CHLOROHYDRATE 20.00%
Clinique Antiperspirant
FDA Label NDC 49527-571
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 Inc for the product Clinique Antiperspirant (NDC 49527-571). 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 otc - active ingredient, otc - purpose, warnings, otc - keep out of reach of children, indications & usage, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
USES: DECREASES UNDERARM PERSPIRATION
Warnings
WARNINGS:
- FOR EXTERNAL USE ONLY
- DO NOT USE ON BROKEN SKIN
- STOP USE IF RASH OR IRRITATION OCCURS
- 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.
Indications & Usage
DIRECTIONS: APPLY TO UNDERARMS ONLY.
Inactive Ingredient
inactive ingredients: water[] urea [] silica [] alcohol denat. [] glycine [] aluminum chloride [] butyl stearate [] sodium lauroyl sarcosinate [] alcloxa [] benzethonium chloride [] trisodium edta [] methylparaben [] propylparaben [] butylparaben iln27821
Package Label.Principal Display Panel
PRINCIPAL DISPLAY PANEL:
CLINIQUE
anti-perspirant deodorant roll-on
ALUMINUM CHLOROHYDRATE
2.5FL OZ./ 70ML
CLINIQUE LABORATORIES, DIST.
NEW YORK, NY 10022
6183
CLINIQUE.COM
Folding Carton (6183 Final)
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