Otc - Active Ingredient
Isopropyl Alcohol 70% v/v
Isopropyl Rubbing Alcohol Wipe
FDA Label NDC 77093-301
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vincit Zee for the product Isopropyl Rubbing Alcohol Wipe (NDC 77093-301). 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, indications & usage, otc - ask doctor, warnings, otc - stop use, otc - when using, 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
First aid antiseptic
Indications & Usage
- first aid to help prevent the risk of infection in minor cuts, scrapes and burns
Otc - Ask Doctor
Ask a doctor before use if you have
- deep or puncture wounds, animal bites or serious burns
Warnings
- For external use only
- flammable, keep away from heat or flame
Otc - Stop Use
Stop use and ask a doctor if condition persists or gets worse
Otc - When Using
- do not get into eyes
- do not apply over large areas of the body
- do not use longer than one week unless directed by a doctor
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Dosage & Administration
- clean affected area
- apply small amount of this product on the area 1-3 times daily
- if bandaging, let dry first
- may be covered with a sterile bandage
Storage And Handling
Do not apply internally. Keeper canister tightly closed and at controlled room temperature. Hold away from face when opening.
Inactive Ingredient
purified water
Package Label.Principal Display Panel
120 wet wipes NDC: 77093-301-05
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