Active Ingredient
ETHYL ALCOHOL 62%
Premium Hand Sanitizer
FDA Label NDC 11673-263
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Target for the product Premium Hand Sanitizer (NDC 11673-263). 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, when using this product, stop using this product and ask 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
ANTISEPTIC
Uses
TO HELP REDUCE BACTERIA ON THE SKIN.
Warnings
FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.
When Using This Product
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.
Stop Using This Product And Ask Doctor If
IRRITATION OR REDNESS DEVELOPS AND LASTS FOR MORE THAN 72 HOURS.
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Directions
WET HANDS THOROUGHLY AND RUB TOGETHER UNTIL DRY.
Questions Or Comments
1-800-910-6874
Inactive Ingredients
WATER, GLYCERIN, ISOPROPYL ALCOHOL, PROPYLENE GLYCOL, TOCOPHERYL ACETATE, RETINYL PALMITATE, AMINOMETHYL PROPANOL, BENZOPHENONE-4, CARBOMER, FRAGRANCE, MANNITOL, CELLULOSE, ULTRAMARINES (CI 77007), HYDROXYPROPYL METHYLCELLULOSE, RED 33 (CI 17200), RED 4 (CI 14700), YELLOW 5 (CI 19140).
Package Label.Principal Display Panel
Image Of Premium Hand Sanitizer (Upup2)
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