Antiperspirant Spray
FDA Label NDC 53329-010

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 Antiperspirant (NDC 53329-010). 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 13% Anhydrous Basis

Purpose

Antiperspirant

Uses

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

Warnings

  • For external use only.
  • Flammable, keep away from fire or flame.

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 accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply to underarms only.

Inactive Ingredients

Fragrance, Isopropyl Alcohol, PEG-40 Hydrogenated Castor Oil, Propylene Glycol, Water

Package/Label Principal Display Panel

NDC 53329-010-13

MedSpa

pump spray

anti-perspirant

Non-Aerosol

2 fl oz (59 mL)

* Please review the disclaimer below.