Instant Hand Sanitizer Classic
FDA Label NDC 76114-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Aidi Cosmetics Co., Ltd for the product Instant Hand Sanitizer Classic (NDC 76114-001). 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 other, active ingredient(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

NA

Active Ingredient(S)

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame

For external use only.

Otc - When Using

When using this product do not use in or near the eyes. In case of contact with eyes, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or rash appears and lasts

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.

Directions

Place enough product in your palm to thoroughly spread on both hands and rub into the skin untill dry

Children under 6 years of age shoud be supervised when using thisĀ 

Other Information

Do not store above 106F (41C)

May discolor certain fabrics or surfaces

Inactive Ingredients

Water, aloe barbadensis leaf extract, carbomer, fragrance, propylene glycol, glycerin, tocopheryl acetate, Triethanolamine

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