(Active Ingredient):
Alcohol 75% v/v
Rubbing Alcohol
FDA Label NDC 78163-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Cheerflor Cosmetics Co., Ltd. for the product Rubbing Alcohol (NDC 78163-002). 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):, (purpose):, (inactive ingredient):, (use):, (directions):, (warnings):, when using this product, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
(Purpose):
Sterilization
(Inactive Ingredient):
Aqua
(Use):
hand and skin disinfection.
(Directions):
for skin external use.
(Warnings):
For external use only.
Flammable. Keep away from fire or flame.
When Using This Product
do not use in or near the eyes. In case of contact, rinse eyes the thoroughly with water.
Stop Use And Ask A Doctor
if irritation or rash appears and lasts.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Package Labeling:
Label (Label)
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