Active Ingredient(S)
Ethyl Alcohol 75% v/v
Hand Sanitizer
FDA Label NDC 78565-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Meixin Beauty & Health Care Products Co., Ltd. for the product Hand Sanitizer (NDC 78565-002). 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, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Warnings
For external use only. Only on hands
Flammable, keep away from fire or flam
Do Not Use
Do not use in or near eyes In case of contact
rinse thoroughly with water
Otc - When Using
/
Otc - Stop Use
Stop use and ask a doctor if irritation and redness
develop and persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
If swallowed, get medical help or contact a
Poison Control Center right away
Directions
Put enough product on palm and rub hands until drya
Children under 6 years of age should be supervised while using this
product
Other Information
/
Inactive Ingredients
Auqa(water), glycerin, parfum
Indications & Usage
To decrease bacteria on skin without soap or water
Recommended for repeated use
Package Label - Principal Display Panel
60 (60)
59 (59)
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