Axe Crew Cut
FDA Label NDC 64942-1161
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 Crew Cut (NDC 64942-1161). 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 - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Indications & Usage
Warnings
Otc - When Using
When using this product keep out of eyes. Rinse with water to remove.
Otc - Stop Use
Stop use and ask a doctor if rash or irritation develops.
Otc - Keep Out Of Reach Of Children
Dosage & Administration
Inactive Ingredient
Otc - Questions
Package Label.Principal Display Panel
Axe Buzz SPF15 back 1
Axe Buzz SPF15 back 2
Axe Buzz SPF15 back 3
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