Hand Sanitizer Original
FDA Label NDC 76114-004

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 Hand Sanitizer Original (NDC 76114-004). 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.

Label Section Quick Index

Other

NA

Active Ingredient(S)

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria on the skin

When water, soap, and towel are not available

Recommended for repeaded use

Warnings

For external use only.

Flammable. Keep away from fire or flame

Otc - When Using

Do not apply around eyes

Do not use in ears and mouth

When using this product avoid contact with eyes. In case of contact, flush eyes with water.

Otc - Stop Use

Stop use and ask a doctor if redness or irritation develops and persists 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.

Directions

Pump as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Other Information

Store at 20C (68-77F)

May discolor fabrics

Inactive Ingredients

Water, carbomer, triethanolamine, glycerin, aloe barbadensis leaf jiuce

Package Label.Principal Display Panel

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