Hand Sanitizer
FDA Label NDC 77753-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Shandishi Biological Technology Co., Ltd. for the product Hand Sanitizer (NDC 77753-004). 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 drug facts, active ingredient, purpose, uses, warnings, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

For Hand Sanitizing

Warnings

Warnings: For external use only-hands.
Flammable: Keep away from heat and flame.
When using this product Keep out of eyes. In case of
contact with eyes, flush thoroughly with water.●Avoid contact with
broken skin.●Do not inhale or ingest.
Stop use and ask a doctor
if skin irritation develops.

Keep Out Of Reach Of Children.

Keep out of reach of children

If swallowed, get medical help or call a Poison Control Center right away.

Directions

Wet hands thoroughly with product and allow to
dry without wiping●For children under 6 use only under adult
Supervision.●Not recommended for infants.

Other Information

1 Do not store above 105°F
1 May discolor some fabrics

Inactive Ingredients

Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl
Acetate, Triethanolamine, Water.

* Please review the disclaimer below.