Isopropyl Alcohol
FDA Label NDC 50730-3002

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 (NDC 50730-3002). 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, otc - ask doctor/pharmacist, otc - when using, stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Isopropyl Alcohol 70% v/v

Purpose

Antiseptic

Use

  • For preparation of the skin prior to injection

Warnings

  • For external use only
    • Flammable, keep away from fire or flame


Do Not Use

  • With electrocautery procedures
  • In the eyes

Otc - Ask Doctor/Pharmacist


Otc - When Using


Stop Use

if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

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 and discard.

Other


Other Information

Store at room temperature 15°- 30° C (59° - 86° F)

Inactive Ingredient

Purified water

Otc - Questions


Package Information

TRIADCat. No. 10-3002NDC 50730-3002-0Alcohol Prep Pads, LargeAntiseptic for preparation of the skin prior to injection70% Isopropyl Alcohol, v/v100 Prep PadsTriad Group, Inc.700 West North Shore DriveHartland, WI 53029MADE IN USAwww.triad-group.net1-800-288-1288

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