Mommy Tillia
FDA Label NDC 10096-0238

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 Mommy Tillia (NDC 10096-0238). 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 - ask doctor, otc - keep out of reach of children, general precautions, 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 Ingredient

Ethyl Alcohol 64.7%.......................

Otc - Purpose

               Purpose

...............antiseptic

Indications & Usage

Uses

  • for handwashing to decrease bacteria on the skin

Warnings

WarningsFOR EXTERNAL USE ONLY.Do not use in the eyes. If contact occurs, flush eyes with water.

Otc - Ask Doctor

Stop use and ask a Health Care Practitioner if

  • irritation and redness develop

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. Flammable until dry. Keep away from heat and open flame.

General Precautions

Other informationDO NOT USE IF SEAL IS BROKEN.

Inactive Ingredient

INACTIVE INGREDIENTS: WATER/EAU
     GLYCERIN
     CARBOMER
     TRIETHANOLAMINE
     HYDROXYPROPYLCELLULOSE
     PARFUM/FRAGRANCE

Otc - Questions

Questions? Call 1-800-FOR-AVON or 1-800-265-AVON in Canada

Dosage & Administration

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.
  • Supervise children in the use of this product.

* Please review the disclaimer below.