Active Ingredient(S)
Ethyl Alcohol 75%
Alcohol Wipes
FDA Label NDC 79683-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hefei Inridy Medical Products Co., Ltd for the product Alcohol Wipes (NDC 79683-003). 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, use, warnings, do not use, otc - when using, otc - stop use, otc - 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
Purpose
Antibacterial
Use
Kills bacteria on surfac
Warnings
For external use only
Do Not Use
/
Otc - When Using
When using this product, do not get into eyes. If contact occurs, rinse thoroughly with water
Otc - Stop Use
Stop using and ask a doctor if irritation or rash develops and continues 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
Remove cap from barrel.
Remove foil seal.
Locate the centre sheet from the middle of the roll pull through the shaped hole.
Replace the cap to avoid evaporation
Supervise children under 6 years of age when using this product to avoid swallowing
Other Information
Store below 25 degree Celsius.
Avoid excessive heat
Inactive Ingredients
Water, Phenoxyethanol, Benzalkonium Chloride, Ethylhexylglycerin, Propylene Glycol, Didecyl dimethyl ammonium chloride, Glycerin
* Please review the disclaimer below.
