Genuine First Aid Hand Sanitizer Ethyl Alcohol Gel
FDA Label NDC 50814-063
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gfa Production (xiamen) Co., Ltd. for the product Genuine First Aid Hand Sanitizer Ethyl Alcohol (NDC 50814-063). 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 70% v/v
Purpose
Antiseptic
Uses
- For hand washing to decrease bacteria on the skin that may cause disease.
- Recommended for repeated use.
Warnings
Flammable, keep away from fire or flame
For external use only.
Intended for use exclusively by adults.
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 todry without wiping.
Other Information
Store at 15° to 25°C (59° to 77°F)
Inactive Ingredients
Acrylic acid Polymers, Propylene glycol, Trolamine, Purified water.
Package Labeling:473Ml
Bottle (Bottle)
Package Labeling:946Ml
Bottle7 (Bottle7)
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