Imari Seduction
FDA Label NDC 10096-0196

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Avon Products, Inc. for the product Imari Seduction (NDC 10096-0196). 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, indications & usage, warnings, otc - when using, otc - ask doctor/pharmacist, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active/

Medicinal ingredient         Purpose
Aluminum Chlorohydrate
14.5%, anhydrous........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/Pharmacist

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 / NON-MEDICINAL
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

* Please review the disclaimer below.