Every Fresh Hand Sanitizer
FDA Label NDC 76772-014

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi for the product Every Fresh Hand Sanitizer (NDC 76772-014). 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, purpose, uses, 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

Drug Facts

Active Ingredient

Ethyl Alcohol, 70% v/v

Purpose

Antiseptic

Uses

  • To help reduce bacteria on the skin
  • For use when soap and water are not available

Warnings

For external use only. Flammable, keep away from fire or flame.

Otc - When Using

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if significant irritation or sensitization develops.

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

-Put enough product on your palm to cover hands and rub your hands together until dry.

-Children under 6years should be supervised when using this product.

Other Information

Store below 43°C (110°F)

May discolor certain fabrics

Inactive Ingredients

carbomer, aloe barbadensis leaf juice, aminomethyl propanol, glycerin, water, tocopheryl acetate (Vit E).

Package Label.Principal Display Panel

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