Otc - Active Ingredient
Active ingredient
Aluminum Chlorohydrate
14.5%, anhydrous...........
Black Suede
FDA Label NDC 10096-9182
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by New Avon Llc for the product Black Suede (NDC 10096-9182). 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 - ask doctor, 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
Purpose
.............Antiperspirant
Indications & Usage
Uses
• reduces underarm perspiration
• lasts 24 hours
Warnings
Warnings
For external use only
Otc - When Using
When using this product
• do not apply to broken skin
• stop use if rash or irritation develops
Otc - Ask Doctor
Ask a doctor before use
• if you have kidney disease
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
Inactive Ingredient
INACTIVE INGREDIENTS :
WATER/EAU, STEARETH-2,
PPG-15 STEARYL ETHER,
DICAPRYL ADIPATE, PARFUM/
FRAGRANCE, STEARETH-20,
ISOPROPYL PALMITATE.
Otc - Questions
Questions? Call 1-800-FOR-AVON
or 1-800-265-AVON in Canada
Package Label.Principal Display Panel
Image Of Pdp (Blacksuedepdp)
Image Of Label (1021012p Blksuede Bb1)
Image Of Label (1021012p Blksuede Bb2)
* Please review the disclaimer below.
