Premium Gel Alcohol Hand Sanitizer
FDA Label NDC 71907-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dade Paper & Bag, Llc for the product Premium Gel Alcohol Hand Sanitizer (NDC 71907-200). 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, uses:, warnings:, otc - keep out of reach of children, directions:, other information:, 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
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 or condition persists for more than 72 hours.
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:
Wet hands thoroughly with product and allow to dry without wiping
For children under 6, use only under adult supervision ■ Not recommended for infants.
Other Information:
Do not store above 105°F ■ May discolor some fabrics
Harmful to wood finishes and plastics.
Inactive Ingredients
Deionized Water, Aloe Vera Gel (Aloe Barbadensis Leaf Juice), Carbomer, Triethanolamine, Vitamin E (Tocopheryl Acetate).
Packaging
Premium1 (71907200 2)
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