Isopropyl Alcohol
FDA Label NDC 50730-3101

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 50730-3101). 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, ask a doctor, 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

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

Ask A Doctor

If conditions persist for more than 72 hours

Otc - Ask Doctor/Pharmacist


Otc - When Using


Stop Use

if irritation and redness develop.

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

TRIADCat. No. 10-3101NDC 50730-3101-0STERILEAlcohol Prep Pads, Medium70% Isopropyl Alcohol, v/vAntiseptic for preparation of the skin prior to injectionLatex Free200 Prep PadsTriad Group, Inc.700 West North Shore DriveHartland, WI 53029MADE IN USAwww.triad-group.net1-800-288-1288

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