Active Ingredient
Isopropyl Alcohol 70%, USP
Purify Instant Hand Sanitizer
FDA Label NDC 79660-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Purify Solutions Inc. for the product Purify Instant Hand Sanitizer (NDC 79660-001). 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, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
Use as a hand sanitizer in the absence of soap and water, to reduce bacteria on the skin which may cause illness.
Recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from heat or flame.
When Using This Product:
- Do not use in or near the eyes, or inhale.
- In case of contact, rinse eyes thoroughly with water.
Stop use and contact your doctor if a rash or irritation appear and persist at the site of contact.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help immediately or contact a poison control center immediately.
Directions
- Spray hand sanitizer onto hands or enough to thoroughly cover hands. Rub hands together briskly for 30 seconds or until dry.
- Children under 6 years of age must be supervised when using the product
Other Information
- Do not store above 110°F (43°C). May discolor certain fabrics or substances.
Inactive Ingredients
aloe (aloe barbadensis) juice, carbomer 940NF, dl-alpha-tocopheryl acetate, triethanolamine glycerin.
Package Label - Principal Display Panel
Label (Label)
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