Active Ingredient(S)
Alcohol 75% v/v. Purpose: Antiseptic
Alcohol Wipes
FDA Label NDC 79060-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vara Home Usa Llc for the product Alcohol Wipes (NDC 79060-001). 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 active ingredient(s), purpose, use, warnings, do not use, stop use and ask a doctor, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Alcohol wipes
Use
• For hand santitizing to decrease bacteria on the skin.
• Apply topically to the skin to help prevent cross contamination.
• Not recommended for repeated use.
• Dries in seconds.
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Do Not Use
in or contact the eyes.
Stop Use And Ask A Doctor
if too much skin irritation and sensitivity develops or increases
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
- 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℃ (59-86°F).
- Lot No. Manufacture date and expiration date can be found on package.
Inactive Ingredients
water
Package Label - Principal Display Panel
1 wipe NDC: 79060-001-01
Pdp (01)
10 wipes NDC: 79060-001-02
Pdp (02)
50 wipes NDC: 79060-001-03
Pdp (03)
* Please review the disclaimer below.
