Active Ingredient
ETHYL ALCOHOL 62%
Careone
FDA Label NDC 41520-220
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by American Sales Company for the product Careone (NDC 41520-220). 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 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
ANTISEPTIC
Uses
TO HELP REDUCE BACTERIA ON THE SKIN.
Warnings
FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROM FIRE OR HEAT SOURCE.
When Using This Product
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.
Stop Using This Product And Ask A Doctor If
IRRITATION OR REDNESS DEVELOPS AND LASTS.
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.
Other Information
STORE AT ROOM TEMPERATURE BELOW 110F (43C).
Inactive Ingredients
WATER, GLYCERIN, ISOPROPYL MYRISTATE, PROPYLENE GLYCOL, TOCOPHERYL ACETATE, AMINOMETHYL PROPANOL, CARBOMER, FRAGRANCE (PARFUM).
Label Copy
Image Of The Label (18112l)
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