Active Ingredient(S)
Ethyl Alcohol 70% v/v
Xtreme Personal Care Hand Sanitizer
FDA Label NDC 52989-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Taizhou Yadai Daily-use Co., Ltd. for the product Xtreme Personal Care Hand Sanitizer (NDC 52989-004). 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, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
Hand sanitizer to help decrease bacteria on the skin
Warnings
For external use only. Flammable. Keep away from heat or flame
When using this product, keep out of eyes, ears or mouth. In case of contact with eyes, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs, these may be signs of serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get immediate medical help or contact a Poison Control Center right away.
Directions
- Apply onto hands/skin, rub until dry
Inactive Ingredients
Water, Triethanolamine, Carbomer, Aloe Barbadensis Leaf Juice, Glycerin, Frangrance, Propylene Glycol, Tocopheryl Acetate
Package Label.Principal Display Panel
Image Description (5f975c10c4cba09153dfc6a58da3b32)
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