Directions:
Spray enough product on hands to cover all surfaces. Rub hands together until dry.
Alcohol Hand Sanitizer
FDA Label NDC 70445-412
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Webb Business Promotion for the product Alcohol Hand Sanitizer (NDC 70445-412). 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 directions:, active ingridient, inactive ingredients:, otc - keep out of reach of children, otc - do not use, warnings, indications & usage, otc - purpose, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingridient
Ethyl Alcohol (62%).
Inactive Ingredients:
Deionized Water, Glycerin, Propylene Glycol, Tocopherol, Citrus Fragrance, Aloe Vera.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Do Not Use
Do not use on children less than 2 months of age. Do not use on open skin wounds.
Warnings
For external use only. Flammable. Keep away from heat or flame. Keep out of eyes, eras & mouth. In case of contact with eyes, rinse eyes thoroughly with water. If swallowed, get medical help or contact a Poison Control Center right away.
Indications & Usage
Antibacterial hand sanitizer spray.
Otc - Purpose
Antiseptic.
Package Label.Principal Display Panel
4ozan-page-001 (4ozsan Page 001)
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