1. Home
  2. Labeler Index
  3. Johnson & Johnson Consumer Inc.
  4. 69968-0055
  5. NDC Package Code: 69968-0055-2 Neosporin Plus Pain Relief First Aid Antibiotic/pain Relieving

NDC Package 69968-0055-2 Neosporin Plus Pain Relief First Aid Antibiotic/pain Relieving

Neomycin Sulfate,Polymyxin B Sulfate,And Pramoxine Hydrochloride Cream Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
69968-0055-2
Package Description:
1 TUBE in 1 CARTON / 14.2 g in 1 TUBE
Product Code:
69968-0055
Proprietary Name:
Neosporin Plus Pain Relief First Aid Antibiotic/pain Relieving
Non-Proprietary Name:
Neomycin Sulfate, Polymyxin B Sulfate, And Pramoxine Hydrochloride
Substance Name:
Neomycin Sulfate; Polymyxin B Sulfate; Pramoxine Hydrochloride
Usage Information:
Do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 caplets every 6 hours while symptoms lastdo not take more than 6 caplets in 24 hours, unless directed by a doctordo not use for more than 10 days unless directed by a doctorchildren under 12 yearsask a doctor do not use more than directed adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: ask a doctor adults and children 2 years of age and older:clean the affected areaapply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times dailymay be covered with a sterile bandagechildren under 2 years of age: ask a doctor
11-Digit NDC Billing Format:
69968005502
NDC to RxNorm Crosswalk:
  • RxCUI: 1087026 - diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Cream
  • RxCUI: 1087026 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Cream
  • RxCUI: 1087026 - diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Cream
  • RxCUI: 1111764 - Benadryl Itch Stopping, Extra Strength 2 % / 0.1 % Topical Cream
  • RxCUI: 1111764 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Cream [Benadryl Itch Stopping]
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Johnson & Johnson Consumer Inc.
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    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):
  • NEOMYCIN SULFATE 3.5 mg/g
  • POLYMYXIN B SULFATE 10000 [USP'U]/g
  • PRAMOXINE HYDROCHLORIDE 10 mg/g
    • Pharmacologic Class(es):
  • Aminoglycoside Antibacterial - [EPC] (Established Pharmacologic Class)
  • Aminoglycosides - [CS]
  • Polymyxin-class Antibacterial - [EPC] (Established Pharmacologic Class)
  • Polymyxins - [CS]
    • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    12-01-2009
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    69968-0055-11 TUBE in 1 CARTON / 28.3 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69968-0055-2?

    The NDC Packaged Code 69968-0055-2 is assigned to a package of 1 tube in 1 carton / 14.2 g in 1 tube of Neosporin Plus Pain Relief First Aid Antibiotic/pain Relieving, a human over the counter drug labeled by Johnson & Johnson Consumer Inc.. The product's dosage form is cream and is administered via topical form.

    Is NDC 69968-0055 included in the NDC Directory?

    Yes, Neosporin Plus Pain Relief First Aid Antibiotic/pain Relieving with product code 69968-0055 is active and included in the NDC Directory. The product was first marketed by Johnson & Johnson Consumer Inc. on December 01, 2009 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 69968-0055-2?

    The 11-digit format is 69968005502. 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 5-4-1 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
    5-4-169968-0055-25-4-269968-0055-02