Carpe Antiperspirant Underarm Lotion
FDA Label NDC 52261-4721

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 Underarm (NDC 52261-4721). 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 - Active Ingredient

Active Ingredient                                                      Purpose
Aluminum Sesquicholorhydrate 15% .......................Anti-perspirant

Otc - Purpose

Anti-perspirant

Use

  • Reduces underarm 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

  • Apply to underarms only
  • Rotate knob to dispense product and rub in vigorously 
  • For best results, apply every night before bed and an additional two times per day for at least four weeks

Inactive Ingredients

Water, Glyceryl Stearate SE, Silica, Silica Silylate, Glycerin, Dimethicone, Ethylhexyl Palmitate, Cetyl Alcohol, Cetostearyl Alcohol, Isopropyl Myristate, Eucalyptus Oil, Phenoxyethanol, Hydroxypropyl Methylcellulose, Ethylhexylglycerin, Sodium Hydroxide

Questions?

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