Hand Sanitizer
FDA Label NDC 77070-700

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Goodfibers for the product Hand Sanitizer (NDC 77070-700). 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 active ingredient, purpose, uses, warnings, when using, stop use, keep out of reach, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient

→ Purpose

→ Uses

→ Warnings

→ When Using

→ Stop Use

→ Keep Out Of Reach

→ Directions

→ Other Information

→ Inactive Ingredients

→ Pdp

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

Hand sanitizer to decrease bacteria on the skin
Recommended for repeated use

Warnings

For external use only Flammable

Keep away from fire or flame

When Using

When using this product:

Do not use in or near eyes

If contact occurs, rinse eyes thoroughly with water.

Stop Use

Stop use and ask a doctor

If irritation and redness persist for more than 72 hours.

Keep Out Of Reach

Keep out of reach of children

In case of accidental ingestion, seek medical attention or contact a poison control centerimmediately

Directions

Place enough product on your palm to thoroughly spread on both hands and rub into the skin until dry.
Children under six years of age should be supervised when using this product.