Active Ingredient(S)
Ethyl Alcohol 75% Purpose: Antimicrobial
Primeauty
FDA Label NDC 75186-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Huizhou Duomei Daily Necessities Co., Ltd. for the product Primeauty (NDC 75186-004). 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(s), purpose, uses, warnings, otc - stop use, 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
Purpose
Antimicrobial
Uses
- For hand washing to decrease bacteria on the skin
- Recommended for repeated use
Warnings
- Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
- for external use only.
- Flammable, keep away from heat and flame
Otc - Stop Use
- Stop use and ask a doctor if
- irritation and redness develop and persist for more than 72 hours
- Swallowed, get medical help or contact a poison control center right away.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be supervised in use of this product.
Directions
- Put enough product on hands to cover all surfaces. Rub hands together until dry.
- Children under 6 years of age should be supervised when using this product.
Other Information
- Store below 110F (43C)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water, Glycerin, Carbomer, Triethanolamine, Tocopheryl Acetate, Aloe
* Please review the disclaimer below.
