My Little Pony Antibacterial Hand Sanitizer With Moisturizers
FDA Label NDC 40104-204

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Pulisi Daily Chemical Products Co., Ltd. for the product My Little Pony Antibacterial Hand Sanitizer With Moisturizers (NDC 40104-204). 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 - keep out of reach of children, other, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active ingredient
Ethyl Alcohol 62% v/v

Otc - Purpose

Purpose
Antiseptic

Indications & Usage

Uses • hand sanitizer to help reduce bacteria on the skin, when water, soap and towel are not available. • recommended for repeated use.

Warnings

Warnings Flammable Keep away from fire or flame For external use only

Otc - When Using

When using this product • avoid contact with eyes • in case of eye contact flush eyes with water. • stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. Children must be supervised in use of this product.

Other

Other Information • store at 20°C(68-77°F). • May discolor fabrics.

Dosage & Administration

Directions •Pump as needed into your palm to thoroughly spread on both hands. •rub into the skin until dry.

Inactive Ingredient

Inactive ingredients caprylyl glycol, carbomer, fragrance, glycerin, isopropyl alcohol, isopropyl myristate, PEG-40 hydrogenated castor oil, phenoxyethanol, propylene glycol, tocopheryl acetate, triethanolamine, water.

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