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  5. NDC Package Code: 60913-207-02 Alcohol Prep Pads

NDC Package 60913-207-02 Alcohol Prep Pads

Isopropyl Alcohol Swab Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
60913-207-02
Package Description:
200 PACKET in 1 CARTON / 1 mL in 1 PACKET
Product Code:
60913-207
Proprietary Name:
Alcohol Prep Pads
Non-Proprietary Name:
Isopropyl Alcohol
Substance Name:
Isopropyl Alcohol
Usage Information:
For preparation of the skin prior to injection
11-Digit NDC Billing Format:
60913020702
NDC to RxNorm Crosswalk:
  • RxCUI: 797544 - isopropyl alcohol 70 % Medicated Pad
  • RxCUI: 797544 - isopropyl alcohol 0.7 ML/ML Medicated Pad
  • RxCUI: 797544 - isopropyl alcohol 70 % Topical Cloth
  • RxCUI: 797544 - isopropyl alcohol 70 % Topical Swab
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Phoenix Healthcare Solutions Llc
    Dosage Form:
    Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • ISOPROPYL ALCOHOL 70 mL/100mL
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-16-2021
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 60913-207-02?

    The NDC Packaged Code 60913-207-02 is assigned to a package of 200 packet in 1 carton / 1 ml in 1 packet of Alcohol Prep Pads, a human over the counter drug labeled by Phoenix Healthcare Solutions Llc. The product's dosage form is swab and is administered via topical form.

    Is NDC 60913-207 included in the NDC Directory?

    Yes, Alcohol Prep Pads with product code 60913-207 is active and included in the NDC Directory. The product was first marketed by Phoenix Healthcare Solutions Llc on August 16, 2021 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 60913-207-02?

    The 11-digit format is 60913020702. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-260913-207-025-4-260913-0207-02