Axe
FDA Label NDC 64942-1101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Conopco Inc. D/b/a Unilever for the product Axe (NDC 64942-1101). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - ask doctor, otc - stop use, otc - 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

Otc - Active Ingredient

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY(17.8%)

Otc - Purpose

Purposeanti-perspirant

Indications & Usage

Uses· reduces underarm wetness· 24 hour protection

Warnings

WarningsFor external use only

Otc - Do Not Use

Do not use on broken skin

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease

Otc - Stop Use

Stop use if rash or irritation occurs

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions· apply to underarms only· turn dial to raise product· to ensure product appears clear on skin, do not overapply· replace cap

Inactive Ingredient

Inactive ingredients

Cyclopentasiloxane, PPG-14 Butyl Ether, Stearyl Alcohol, Hydrogenated Castor Oil, PEG-8 Distearate, Talc, Fragrance (Parfum), BHT

Otc - Questions

Questions?

Call toll-free 1-800-450-7580

Package Label.Principal Display Panel

Phoenix 2.7 oz PDP

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