Anti-perspirant Deodorant Spray
FDA Label NDC 68599-2304

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Mckesson Medical-surgical Inc. for the product Anti-perspirant Deodorant (NDC 68599-2304). 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 other, active ingredient, purpose, use, otc - keep out of reach of children, otc - do not use, otc - stop use, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

FOR EXTERNAL USE ONLY.

Active Ingredient

Aluminum Chlorohydrate, Anhydrous Basis 13%

Purpose

Antiperspirant

Use

Reduces underarm wetness.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Otc - Do Not Use

Do not use on broken skin.

Otc - Stop Use

Stop use if rash or irritation occurs.

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

Directions

Hold two inches from underarm and spray. Use daily for best results.

Inactive Ingredients

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

* Please review the disclaimer below.