Zing Hand Sanitizer
FDA Label NDC 74953-415
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zing Brothers Llc for the product Zing Hand Sanitizer (NDC 74953-415). 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 drug facts, active ingredients:, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients:
Alcohol 80%
Purpose
(Antiseptic)
Uses
Hand Sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only. Flammable. Keep away from heat or flame. Do not use in children less than 2 months of age or on open skin wounds. When using this product, keep out of eyes, ears and mouth. In case of contact with eyes, rinse with soap and water. Stop use and ask a doctor if irritation or rash occurs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center.
Directions
Place enough product on hands to cover surface. Rub hands together until dry. Supervise children under 6 years of age to avoid swallowing.
Other Information
Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
Glycerin, Hydrogen Peroxide, Carbopol ETD, Triisopropanolamine, Water
Packaging
Image Description (Label2)
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