Active Ingredient
Ethyl alcohol 62%
Zetta Hand Gel
FDA Label NDC 74170-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dbk Korea Co., Ltd. for the product Zetta Hand Gel (NDC 74170-001). 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, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
- Hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable. Keep away from fire or flame.
For external use only
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 doctor if irritation or rash appears and lasts
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 nough produt in your palm to cover hands and rub hands together briskly until dry.
- Children under 6 years of age should be supervised when using this product
Other Information
- Store below 110°F (43°C)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Carbomer, Triethanolamine, Glycerin, Butylene Glycol, Aloe Vera Gel, D-Panthenol, Tocopherol, Dipotassium Glycyrrhizate, Fragrance, Purified Water
Package Label.Principal Display Panel
Product Label (Zetta)
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