Roll On Anti Perspirant Solution
FDA Label NDC 53329-069

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Medline Industries, Lp for the product Roll On Anti Perspirant (NDC 53329-069). 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, do not use, ask a doctor before use if you have, stop 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

Active Ingredient

Aluminum Chlorohydrate 10% Anhydrous

Purpose

Antiperspirant

Uses

  • reduces underarm perspiration
  • also decreases underarm sweating due to stress

Warnings

For external use only.

Do Not Use

on broken skin

Ask A Doctor Before Use If You Have

kidney disease

Stop Use If

rash or irritation occurs

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

Fragrance, Gylcerin, Hydroxyethylcellulose, Polysorbate 20, Tetrasodium EDTA, Water.

Principal Display Panel

NDC: 53329-069-12

MedSpa

roll-on

anti-perspirant

Alcohol-Free

1.5 fl oz (45 mL)

* Please review the disclaimer below.