Active Ingredient
ETHYL ALCOHOL 65%
Aurora
FDA Label NDC 63148-408
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Apollo Health And Beauty Care for the product Aurora (NDC 63148-408). 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 use 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 DECREASE BACTERIA ON THE SKIN
Warnings
- FOR EXTERNAL USE ONLY
- FLAMMABLE
- KEEP AWAY FROM SOURCE OF HEAT OR FIRE
When Using This Product
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER
Stop Use 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
APPLY A SMALL AMOUNT TO YOUR PALM AND RUB HANDS TOGETHER BRISKLY UNTIL DRY. CHILDREN 6 YEARS OF AGE AND UNDER SHOULD BE SUPERVISED WHEN USING THIS PRODUCT
Other Information
STORE AT A TEMPERATURE BELOW 110°F (43°C)
Inactive Ingredients
WATER (AQUA), PROPYLENE GLYCOL, FRAGRANCE (PARFUM), BENZOPHENONE-4, CARBOMER, GLYCEIRN, TOCOPHERYL ACETATE, AMINOMETHYL PROPANOL, ISOPROPYL MYRISTATE, BLUE 1 (CI 42090), RED 33 (CI 17200)
Questions Or Comments?
1-866-695-3030
Label Copy
Image Of The Label (20300l)
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