Otc - Active Ingredient
Active Ingredient Purpose
Aluminum Sesquicholorhydrate 15% .......................Antiperspirant
Carpe Antiperspirant For Feet
FDA Label NDC 52261-4700
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cosco International, Inc. for the product Carpe Antiperspirant For Feet (NDC 52261-4700). 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, use, warnings, do not use, stop use and ask a doctor if, ask doctor before use if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Anti-perspirant
Use
- Reduces feet perspiration
Warnings
For external use only
Do Not Use
- on broken or irritated skin
Stop Use And Ask A Doctor If
- rash or irritation occurs
Ask Doctor Before Use If
- you have kidney disease
Keep Out Of Reach Of Children
- If swallowed, get medical help or contact a Poison Control Center right away
Directions
- Wash and dry soles throughly before application
- Apply a small, dime-sized amount of Carpe to soles
- Rub Carpe into soles vigorously for 15 seconds
- For best results, apply every night before bed and an additional two times per day for at least four weeks
Inactive Ingredients
Aqua (Water), C12-15 Alkyl Benzoate, Citric Acid, Dimethicone, Ethylhexylglycerin, Eucalyptus Globulus Leaf Oil, Glycerin, Hydroxypropyl Methylcellulose, Isopropyl Alcohol, Isopropyl Myristate, Phenoxyethanol, Polysorbate-20, Silica, Silica Silylate, Sodium Hydroxide, Talc
Questions?
Call 888-621-0135
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