Otc - Active Ingredient
Active Ingredient: Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 52174-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Kleen Products Co., Ltd. for the product Hand Sanitizer (NDC 52174-002). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, inactive ingredient, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Antiseptic
Indications & Usage
Uses: To decrease bacteria on the skin that could cause disease
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
Otc - Stop Use
Stop use and see a doctor if skin irritation develops.
Otc - 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
Inactive Ingredient
Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water
Storage And Handling
Other Information
Do not store above 105F
May discolor some fabric
Harmful to wood finishes and plastics
Dosage & Administration
Directions: Wet hands thoroughly with products and allow to dry without wiping. For children under 6 use only under adult supervision. Not recommended for infants
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