Clarins - Roll-on Deodorant Aluminum Chlorohydrate - Antiperspirant, Long-lasting Alcohol-free Liquid
FDA Label NDC 58668-5981

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Laboratoires Clarins for the product Clarins - Roll-on Deodorant Aluminum Chlorohydrate - Antiperspirant, Long-lasting Alcohol-free (NDC 58668-5981). 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 drug facts:, active ingredient, purpose, uses:, warnings:, do not use, stop use and ask a doctor 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

Drug Facts:

Active Ingredient

ALUMINUM CHLOROHYDRATE

14 %(Anhydrous) w/w

Purpose

Antiperspirant

Uses:

  • Reduces underarm perspiration.

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.

Stop Use And Ask A Doctor If

skin irritation or sensitivity develops or increases.

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:

AQUA/WATER/EAU. DIPROPYLENE GLYCOL. PEG-40 HYDROGENATED CASTOR OIL. METHYL GLUCETH-20. POLYSORBATE 20. HYDROXYETHYLCELLULOSE. PARFUM/FRAGRANCE. PROPANEDIOL. GLYCERIN. BENZYL ALCOHOL. HYDROXYACETOPHENONE. PHENOXYETHANOL. DISODIUM EDTA. CHONDRUS CRISPUS EXTRACT. HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACT. [C0493E]

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