Active Ingredient(S)
Alcohol 75%
Beautimax Hand Sanitizer
FDA Label NDC 76715-006
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 Beautimax Cosmetics Co. Ltd for the product Beautimax Hand Sanitizer (NDC 76715-006). 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, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
Non-medical For extemmaland dally use only. Stop use and ask a doctor imitation and redness develop,. Keep out reach of children, If get into eyes,rinse eyesthroughly with water If swallowed, get medical help or ask.
Do Not Use
- Stop use and ask a doctor imitation and redness develop
Otc - When Using
/
Otc - Stop Use
Stop use and ask a doctor imitation and redness develop
Otc - Keep Out Of Reach Of Children
Keep out reach of children, If get into eyes,rinse eyesthroughly with water If swallowed, get medical help or ask..
Directions
/
Other Information
store in cooldry place dont store ahoye., may discolor somefabrics.humanfulto wood and plastics
Inactive Ingredients
Water/Aqua, Glycerin, PropyleneGlycol, Acrylates/C10-30 Alkyl Acrylate CrosspolymetFragrance/Parfum, Aloe Barbadensis Leaf ExtractDisodium EDTA
Package Label - Principal Display Panel
2 (100ml)
3 (500ml)
4 (60ml)
* Please review the disclaimer below.
