Active Ingredient(S)
Alcohol 75% v/v
Alcohol Wipes
FDA Label NDC 77909-021
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Huihao Medical Technology (zhejiang) Co., Ltd for the product Alcohol Wipes (NDC 77909-021). 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), use, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use
Wipe surface to hel[P redu1Je bacteria that can potientially cause disease.
Do Not Use
In chilldren less than 2 months of age. On open skin wounds
Otc - When Using
Keep out of eyes, ears, and mouth. In case of contact witih eyes, rinse eyes thoroughly with water.
Otc - Stop Use
if irritation or rash occurs. These may be sign of a serious condition.
Otc - Keep Out Of Reach Of Children
if swallowed, get medical help or contact a Poison control Genter right way.
Directions
Rermove and unfold wipe
Wipe surface thoroughly
Dispose of used wipe in trash, do not flush
Other Information
Store between 50-86°F(15-30°C)
Avoid Freezing and excessive heat above 104°F(40°c)
Inactive Ingredients
Purified water
* Please review the disclaimer below.
