Active Ingredient
Ethyl Alcohol 70%
Premium Nature Instant Hand Sanitizer
FDA Label NDC 75821-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Premium Assure Inc for the product Premium Nature Instant Hand Sanitizer (NDC 75821-002). 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, 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 hand sanitizer
Uses
For hand sanitizing to decrease bacteria on skin
Recommended for repeated use
Warnings
For external use only. Flammable. Keep away from fire or flame.
When using this product: Avoid contact with eyes.In case of eye contact, flush eyes with water.
Stop use and ask a doctor if: irritation or redness develops,or if 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.
Directions
Squeeze appropriate amount of sanitizer on to hands and rub together until dry.
Use as needed. For children under 6, use with adult supervision. Not recommended for infants.
Inactive Ingredients
Water, Aloe vera, PEG-6 (and) AMP-Acrylates /Vinyl Isodecanoate Crosspolymer, Vegatable Glycerin, Aminomethylpropanol, Phenoxyethanol, Fragrance
Product Label
Image Description (8oz)
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