Active Ingredient(S)
Alcohol 70%
Alv71 Pure Sanitizer 50ml
FDA Label NDC 76886-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mikolab Co .ltd for the product Alv71 Pure Sanitizer 50ml (NDC 76886-001). 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, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Purpose: Antiseptic
Use
Hand sanitizing to help reduce bacteria on the skin
Warnings
For external use only.
Flammable, keep away from fire or flame.
When using this product, avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Take suitable amount of sanitizer in the hand. Wet thoroughly and rub hands together until dry
Other Information
Store in room temperature 0~30℃
Inactive Ingredients
Water(Aqua), Carbomer, Triethanolamine, Polysorbate 20, Camellia Sinensis Leaf Extract, Glycerin, Tocopheryl Acetate, Fragrance(Parfum)
Package Label - Principal Display Panel
Image Description (50ml)
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