Isopropyl Alcohol Prep Pad
FDA Label NDC 50730-1033

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 Prep Pad (NDC 50730-1033). 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.

Active Ingredient

Isopropyl Alcohol 70% v/v

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

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

NDC 50730-1033-1Kroeger® Quality GuaranteedALCOHOL SWABSSoft Antiseptic Swabs saturated with Isopropyl Alcohol, 70% v/vANTISEPTIC FOR PREPARATION OF THE SKIN PRIOR TO INJECTIONIndividually wrapped140 SWABSQuality GuaranteedIf you are not completely satisfied with this product, return it for a refund or replacement.Comments or Questions?800-632-6900www.kroeger.comDISTRIBUTED BY THE KROEGER CO.,CINCINNATI, OHIO 45202Questions? Please Call: 1-800-491-7448

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