Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 71063-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aiyaya Cloud-commerce Tech Co., Ltd for the product Hand Sanitizer (NDC 71063-001). 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 otc - active ingredient, otc - purpose, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Warnings
Warnings
For external use only.
Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops. If swallowed, get medical help or contact a doctor right away.
Otc - Keep Out Of Reach Of Children
Keep it out of children.
Dosage & Administration
Directions:
Pump as needed into your palms to cover hands. Rub hands together briskly until dry.
Inactive Ingredient
Inactive Ingredients
Water, Aloe Barbadenis Leaf Juice, Glycerin, Propylene Glycol, Fragrance, FD&C Red No.4, FD&C Yellow No. 5
Indications & Usage
Uses
Decrease bacteria on hands
Package Label.Principal Display Panel
Image Of Bottle Label (2344)
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