Otc - Active Ingredient
Active Ingredient: Ethyl Alcohol 62%
Antibacterial Hand Sanitizer
FDA Label NDC 70827-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Top Trenz for the product Antibacterial Hand Sanitizer (NDC 70827-001). 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 otc - active ingredient, otc - purpose, warnings, otc - stop use, otc - keep out of reach of children, inactive ingredient, indications & usage, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose Antiseptic
Warnings
Warnings For external use only. Flammable. Keep away from fire or flame.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a doctor right away.
Inactive Ingredient
Inactive Ingredients Water, Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol, Lactose, Microcrystalline Cellulose, Sucrose, Zea Mays (corn) Starch, Ultramarine Blue CI 77007, Tocopheryl Acetate, Hydroxpropyl Methyl Cellulose, FD&C Red No.4, FD&C Yellow No.5.
Indications & Usage
Uses To help reduce bacteria on the skin.
Dosage & Administration
Directions Pump as needed into your palms to cover hands. Rub hands together briskly unitl dry.
Package Label.Principal Display Panel
Image Of Bottle Label (2570)
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