Active Ingredient
Ethyl Alcohol 70% v/v.
Hand Sanitizer Gel
FDA Label NDC 73143-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jag Alliance, Llc for the product Hand Sanitizer Gel (NDC 73143-001). 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 active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions:, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
To decrease bacteria on the skin that could cause disease. recommended for repeated use.
Warnings
For external use only: hands
Flamable, keep away from heat or flame
When using this product keep out of eyes.In case of contact with eyes, flush throughly with water. Avoid contact with broken skin. Do not inhale or ingest
Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
Apply to hands throughly and allow to dry without wiping.
Supervise children under 6 years of age when using. This product to avoide swallowing or misuse. Not recommended for infants.
Other information: do not store above 105°F, may discolor some fabrics, harmful to wood finishes and plastics.
Inactive Ingredients
Aloe barbadensis leaf juice, Carbomer, Glycerin, Triethanolamine, tocopheryl acetate (Vitamin E), Water
Product Label
Image Description (Label)
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