Alcohol Pad
FDA Label NDC 49348-077

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Mckesson for the product Alcohol Pad (NDC 49348-077). 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

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

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 and discard

Other


Other Information

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

Inactive Ingredient

Purified water

Otc - Questions


Package Information

Sunmark® COMPARE TO B-D® ACTIVE INGREDIENTS*NDC 49348-077-53Alcohol Prep PadsAntiseptic for preparation of the skin prior to injectionIsopropyl alcohol, 70%100 INDIVIDUALLY WRAPPED FOIL PACKETS1.25 X 1.25 IN (2.9 X 3.2 cm)Distributed by McKessonOne Post StreetSan Francisco, CA 94104Money Back Guarantee*This product is not namufactured or distributed by Beckton Dickson, owner of the registered trademark, B-D®.

* Please review the disclaimer below.