Active Ingredient(S)
Alcohol 70% v/v
Viridipharm Hand Sanitizer Antibacterial
FDA Label NDC 73267-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Viridipharm, Llc for the product Viridipharm Hand Sanitizer Antibacterial (NDC 73267-001). 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(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
- Hand sanitizer to help reduce bacteria on the skin that could cause disease
- Recommended for repeated use
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse thoroughly with water.
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 Poison Control Center right away.
Directions
- Place enough product in your palm to thoroughly cover your hands.
- Rub hands together briskly until dry.
- Children under 6 years of age should be supervised when using this product.
Other Information
- Store below 110 F (43 C)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Aloe Barbadensis Leaf Juice (Aloe Vera), Carbomer, Glycerin, Sodium Hydroxide, Water
Questions Or Comments?
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Package Label - Principal Display Panel
8oz (8oz Aloe Retail Label)
20oz (20oz Aloe Retail Label)
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