Antibacterial Hand Sanitizer
FDA Label NDC 90121-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sweda Company Llc for the product Antibacterial Hand Sanitizer (NDC 90121-002). 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 drug facts, active ingredients, purpose, uses:, warnings:, otc - do not use, when using this product,, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Ethyl Alcohol 62%
Purpose
Antiseptic
Uses:
Hand sanitizer to help decrease bacteria on the skin. When water, soap & towel are not available. Recommende for repeated use.
Warnings:
For external use only.
Flammable. Keep away from heat and flame. Do not apply around eyes
Otc - Do Not Use
Do not use in ears & mouth.
When Using This Product,
avoid contact with eyes. In case of contact flush eyes with water.
Stop Use And Ask A Doctor
if redness or irritation develop and persist for more than 72 hours.
Keep Out Of Reach Of Children.
Children must be supervised in use of this product.
Directions:
Squirt as needed into your palms and thoroughly spread on both hands. Rub into skin until dry
Other Information:
Store at 20°C (68°-77°F). May discolor fabrics
Inactive Ingredients:
water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, carbomer, fragrance.
Package Labeling:15Ml
Label (Label)
Package Labeling:30Ml
Label2 (Label2)
Package Labeling:59Ml
Box (Box)
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