Active Ingredient
Ethyl alcohol 75% v/v
Pure Choice Instant Hand Sanitizer
FDA Label NDC 74854-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shanghai Medical Instruments Co.,ltd for the product Pure Choice Instant Hand Sanitizer (NDC 74854-001). 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, use:, warnings, when using this product, stop use and ask a doctor if, 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
Warnings
Flammable. Keep away from fire or flame
For external use only
When Using This Product
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water
Stop Use And Ask A Doctor If
irritation or rash appears and lasts
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
1)Put enough product in your palm to cover hands and rub hands together briskly until dry. 2) Children under 6 years of age should be supervised when using
Inactive Ingredients
Glycerin, Water, Carbomer, aloe extraction, Triethanolamine, Ammonium Lauryl Sulfate, Hyaluronic Acid, Aloe Extract, Parfum
Otc - Questions
Question? 1-866-222-3181.
Package Labeling:
Label (Label)
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