Otc - Active Ingredient
Alcohol 75%. Purpose: Antiseptic
Sanitizing Wipes
FDA Label NDC 79589-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Arch Point Group Llc for the product Sanitizing Wipes (NDC 79589-001). 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 otc - active ingredient, otc - purpose, use(s), warning, when using this product, do not use, stop use and ask a doctor if, 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
Otc - Purpose
Antiseptic
Use(S)
Single Use Wipes for Hands
Warning
- For external use only; hands, general cleansing.
- Does not replace wipes used for medical procedures.
- Flammable; Keep away from fire or flame
- Do not ingest
When Using This Product
- Keep our of eyes. In case of contact with eyes, flush thoroughly with water.
- Avoid contact with broken skin.
Do Not Use
on open skin wounds
Stop Use And Ask A Doctor If
- Irritation and redness develop
- condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep our of reach of children. If swallowed, get medical help or contact a poison control center right away.
Directions
Close properly after dispensing to maintain purity, as alcohol by nature evaporates quickly.
Dispose of properly, DO NOT FLUSH
Other Information
- Keep out of light; store at room temperature 59F-86F.
- Close properly after dispensing to maintain purity, as alcohol by nature evaporates quickly.
- Dispose of properly, DO NOT FLUSH.
Inactive Ingredients
Water, Glycerol
Package Label - Principal Display Panel
50 PCS NDC: 79589-001-01
Pdp (79589 001 01)
* Please review the disclaimer below.
