Vhp Hand Sanitizer
FDA Label NDC 75653-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Valley Herbal Products, Inc. for the product Vhp Hand Sanitizer (NDC 75653-100). 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 ingredient, purpose, directions, uses, warnings, keep out of reach of children, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 70%
Purpose
Antiseptic
Directions
Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.
Uses
To decrease bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
• For external use only: hands.
• Flammable, keep away from fire or flame.
When using this product
• keep out of eyes. In case of contact with eyes, flush thoroughly 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
Keep Out Of Reach Of Children
• If swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredients
Water, triethanolamine, glycerin, Vitamin E, aloe vera gel, carbomer.
Packaging
Image (Vhlabel)
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