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Hand Sanitizer Gel - 65% Alcohol
Drug Facts
Hand Sanitizer Gel - 65% Alcohol
FDA Label NDC 78650-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Juarez Torres Adrian De Jesus for the product Hand Sanitizer Gel - 65% Alcohol (NDC 78650-100). 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, when using this product, otc - stop use, 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(S)
Alcohol 65% v/v.
Purpose
Antiseptic
Use
Hand sanitizer to help reduce bacteria on the skin.
Warnings
Flammable. Keep away from source of heat, fire or flame.
For external use only.
When Using This Product
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops and lasts.
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
- Place enough product in your palm to thoroughly cover your hands and rub hands together until dry.
- Children under 6 years should be supervised when using this product.
Storage
- Store at a temperature below 110°F (43°C)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water, Carbomer, Sodium Bicarbonate
Package Label - Principal Display Panel
8.5 fl. oz. NDC: 78650-100-25
Made in Mexico
* Please review the disclaimer below.
