Antiseptic Hand Sanitizer Ethyl Alcohol Liquid
FDA Label NDC 84219-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by M-star (hubei) Health&care Products Co., Ltd. for the product Antiseptic Hand Sanitizer Ethyl Alcohol (NDC 84219-005). 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 drug facts, active ingredient, purpose, uses, warnings, do not use, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl alcohol 62% v/v
Purpose
Antiseptic
Uses
- For handwashing to decrease bacteria on the skin.
- Recommended for repeated use.
Warnings
Flammable, keep away from fire or flame
For external use only.
Do Not Use
- in the eyes.
Stop Use And Ask A Doctor If
- irritation and redness develop
- condition persists for more than 72 hours
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 at room temperature
Inactive Ingredients
Carbomer, propylene glycol, purified water, titanium dioxide
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Package Labelling:
Label9.jpg (Label9)
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