Active Ingredient
Isopropyl Alcohol 70% v/v
Isopropyl Alcohol Swabs
FDA Label NDC 50730-1020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by H And P Industries, Inc. Dba Triad Group for the product Isopropyl Alcohol Swabs (NDC 50730-1020). 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, purpose, use, warnings, do not use, stop use, otc - ask doctor/pharmacist, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For preparation of the skin prior to an injection
Warnings
For external use only. Flammable, keep away from fire or flame.
Do Not Use
- with electrocautery procedures
- in the eyes
Stop Use
If irritation and redness develop.
Otc - Ask Doctor/Pharmacist
Otc - When Using
Ask A Doctor
If condition persists for more than 72 hours.
Otc - Pregnancy Or Breast Feeding
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wipe injection site vigorously
Other
Other Information
Store at room temperature
Inactive Ingredient
Water
Otc - Questions
Package Information
NDC 50730-1020-0
value plus
ALCOHOL SWABS
Antiseptic for Preparation
of the Skin Prior to Injection
The Triad Group, Inc.
Hartland, WI 53029 USA
Made in USA
Carton (Pl 1020c A A1007)
* Please review the disclaimer below.
