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Drug Facts
Instant Hand Sanitizer Gel
FDA Label NDC 51824-020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by New World Imports, Inc. for the product Instant Hand Sanitizer (NDC 51824-020). 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
Active Ingredient
Ethyl Alcohol 70% v/v
Purpose
Antiseptic
Uses
Hand sanitizer to help reduce bacteria on the skin that could cause disease
Warnings
Flammable. Keep away from fire or flame. For external use only – hands.
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a physician if skin irritation or rash develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If accidently ingested, seek medical help or contact a Poison Control Center immediately.
Directions
Place enough product in your palm to thoroughly cover your hands, rub together briskly until dry. Children under 6 years of age should be supervised when using this product.
Other Information
Store at normal room temperature. May discolor certain fabrics. May be harmful to wood finishes and plastics
Inactive Ingredients
Carbomer, Fragrance, Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Propylene Glycol, Purified Water, Tocopheryl Acetate, Aloe Vera Gel, AMP-95.
* Please review the disclaimer below.
