Active Ingredient
Ethyl Alcohol 75% v/v.
Hemicare Hand Sanitizer
FDA Label NDC 77027-325
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Zuofun Cosmetics Co., Ltd for the product Hemicare Hand Sanitizer (NDC 77027-325). 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, purpose, uses, 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
Antiseptic
Uses
Helps reduce bacteria on the hand
Warnings
For external use only. Flammable. Keep away from fire or flame.
Do not use in the eyes.
Stop use and ask a doctor if irritation and redness develop.
Condition 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
Wet hands thoroughly with product and allow to dry without wiping.
Other Information
Store between 59-86℉(15-30℃).
Avoid freezing and excessive heat above 104℉(40℃)
Inactive Ingredients
Carbomer, Glycerin, Triethanolamine, Water
Product Label
Image Description (Label)
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