Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer Wipes Cloth
FDA Label NDC 76546-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Southern Telecom, Inc. for the product Hand Sanitizer Wipes (NDC 76546-002). 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 active ingredient, purpose, use, warnings, do not use, 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
Use
Hand sanitizer to help reduce bacteria on the skin.
Warnings
Flammable. Keep away from fire or flame. For external use only, do not inhale or ingest
Do Not Use
in or near eyes. In case of contact with eyes, rinse thoroughly with water. Avoid contact with broken skin
Stop Use And Ask A Doctor If
irritation or rash develops and persists for more than 72 hours
Keep Out Of Reach Of Children
If swallowed, get medical help or contact the Poison Control Center immediately.
Directions
- Unfold, and wipe hands thoroughly for about 30 seconds
- For children under 6, use only under adult supervision
- Not recommende for infants
- Dispose of wipe in trash after use. DO NOT flush
Other Information
- Store at room temperature (66°F-77°F)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water, Glycerin, Aloe Barbadensis Leaf Extract, Chamomilla Recutita Flower Extract, Decyl Glucoside, Benzalkonium Chloride, Cetylpyridinium Chloride, Didecyldimonium Chloride
Package Label
Package Label (Clnolgywipes50ctpck)
Container Label (Clnolgywipes150ctcnstr)
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