Sani-choice Instant Hand Sanitizer
FDA Label NDC 80412-070
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sani-choice Corporation for the product Sani-choice Instant Hand Sanitizer (NDC 80412-070). 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, indications & usage, warnings, otc - keep out of reach of children, directions, 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
Indications & Usage
Use- To Sanitize hands without water or rinse
Warnings
For external use only: hands
Flammable, keep away from fire or flame.
■ Keep out of eyes. ■ In case of contact with eyes, flush thoroughly with water ■ Do not inhale or ingest.
If ingested, seek medical help or contact a Poison Control Center right away.
Discontinue if skin irritation or redness occurs
Otc - Keep Out Of Reach Of Children
■ Keep away from children
Directions
Apply Gel to hands; Rub thoroughly; Allow to dry without wiping or rinsing. Store at room temperature
Inactive Ingredients
Water, Acrylic Copolomer, Glycerin, Fragrance, Sodium Hydroxide
Other
FOR ANTISEPTIC USE
Distributed By
Sani- Choice Corporation
4000 West 6th St. Suite B-208
Lawrence, Kansas 66049
MADE IN USA
Packaging
Image (8041207016)
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