Mds Roll-on Anti-perspirant Cream
FDA Label NDC 87119-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Mds Global Fze for the product Mds Roll-on Anti-perspirant (NDC 87119-001). 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 active ingredient, purpose, uses, warnings, directions, inactive ingredients, other information, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Aluminum Chlorohydrate, 15.4 % anhydrous

Purpose

Anti-Perspirant Deodorant

Uses

reduces underarm perspiration

Warnings

  • For external use only 
  • Do not apply to broken skin. Stop use if rash or irritation occurs. 
  • Ask a 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

Inactive Ingredients

DIMETHICONOL, FRAGRANCE, ISOPROPYL MYRISTATE, STEARETH-2, STEARETH-20, WATER.

Other Information

Helps eliminate odor - Anti-stain -Non-stinging. - Non-sticky - Quick-drying

Product Label

Image Description (Image 1 Updated)

Image Description (Image 1 Updated)

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