Active Ingredients
Ethyl Alcohol , 75% v/v
Wet Wipes
FDA Label NDC 90037-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jiangsu Mingsheng Textile Technology Co., Ltd for the product Wet Wipes (NDC 90037-100). 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 ingredients, purpose, use, warnings, do not use, when using this product, 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
Purpose
Antiseptic
Use
- for hand sanitizing to reduce bacteria on skin
Warnings
For external use only. Flammable, keep away from fire or flame
Do Not Use
- with electrocautery procedured
- in the eyes
- if children less than 2 months of age
- on open skin wounds
When Using This Product
- keep out of reach of eyes, ears and mouth
Stop Use And Ask A Doctor If
- irritation or redness develops
- if condition perisits for more than 72 hours, consult a physician
Keep Out Of Reach Of Children
- if swallowed, get medical help or contact a Poison Control Center right away.
Directions
- discard after use
- do not flush
- close the lid properly after use
Other Information
- store at room temperature 15° - 30° ( 59° - 86° F)
- avoid excessive heat
Inactive Ingredients
Aloe Vera Extract, Benzalkonium Chloride, Glycerin , Methyl Phenoxyethanol, Propylene Glycol, Water
Package Label - Principal Display Panel
Image Of Canister Label (100)
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