Axe
FDA Label NDC 64942-1546

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 64942-1546). 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 axe charge up antiperspirant and deodorant - aluminum zirconium tetrachlorohydrex gly stick, drug facts, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active ingredient


Aluminum Zirconium Tetrachlorohydrex GLY (19.0 %)

Purpose

antiperspirant

Uses

• reduces underarm wetness

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

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.

Directions

apply to underarms only

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Talc, PEG-8 Distearate, Fragrance (Parfum), Sodium Starch Octenylsuccinate, Maltodextrin, Hydrolyzed Corn Starch, BHT, Silica

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