Progress Alcohol Wipes
FDA Label NDC 80882-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Truechoicepack, Corp for the product Progress Alcohol Wipes (NDC 80882-001). 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 drug facts, active ingredient, purpose, uses, warnings, 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
Active Ingredient
Ethyl Alcohol 75% by volume
Purpose
Antiseptic
Uses
- For hand washing to decrease bacteria on skin.
- Apply topically to the skin to help prevent cross contamination.
- Not recommended for repeated use.
- Dries in seconds.
Warnings
For external use only.
Flammable, Keep away from fire or flame.
When Using This Product
do not use in or contact the eyes.
Stop Use And Ask A Doctor If
too much skin irritation or sensitivity develops or increases.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
- Open lid, gently pull back resealable label, remove and use wipe as required.
- Reseal back after use to avoid evaporation of alcohol.
Other Information
- Store at room temperature 15°-30°C (59°-86°F).
- Lot No. Manufacture date and Expiration date can be found on package.
Inactive Ingredient
Water
Package Labeling:
Bottle (Bottle)
* Please review the disclaimer below.
