Active Ingredient
Ethyl Alcohol 62.5%
Daily Touch Hand Sanitizer
FDA Label NDC 50523-600
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Volume Distributors, Inc for the product Daily Touch Hand Sanitizer (NDC 50523-600). 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, uses:, warnings:, when using this product, stop use and ask a doctor if, 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
Antiseptic
Uses:
For handwashing to decrease bacteria on the skin. Recommended for repeated use.
Warnings:
For external use only. Flammable, kep away from fire or flame.
When Using This Product
- avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
Stop Use And Ask A Doctor If
- irritation or redness develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center.
Directions:
Wet hands thoroughly with product. Briskly rub hands together until dry. Supervise children in the use of this product.
Other Information:
Store at 20° to 25° C(68° to 77°F).
May discolor certain fabrics.
Inactive Ingredients:
Water (Agua), Glycerol, Aloe Barbadensis Leaf Juice, Carbomer, Triethanolamine
Package Labeling:237Ml
Bottle (Bottle)
Package Labeling:60Ml
Bottle2 (Bottle2)
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