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  5. NDC Package Code: 12258-223-05 Curasore

NDC Package 12258-223-05 Curasore

Pramoxine Hydrochloride Liquid 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:
12258-223-05
Package Description:
1 BOTTLE in 1 CARTON / 15 mL in 1 BOTTLE
Product Code:
12258-223
Proprietary Name:
Curasore
Non-Proprietary Name:
Pramoxine Hydrochloride
Substance Name:
Pramoxine Hydrochloride
Usage Information:
Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily; avoid moistening area for 2 to 3 minutes following application. Children under 2 years of age: consult a doctor.
11-Digit NDC Billing Format:
12258022305
NDC to RxNorm Crosswalk:
  • RxCUI: 1294034 - pramoxine HCl 1 % Topical Solution
  • RxCUI: 1294034 - pramoxine hydrochloride 10 MG/ML Topical Solution
  • RxCUI: 1294034 - pramoxine hydrochloride 1 % Topical Solution
  • RxCUI: 2109512 - CURASORE 1 % Topical Solution
  • RxCUI: 2109512 - pramoxine hydrochloride 10 MG/ML Topical Solution [Curasore]
    • Product Type:
    Human Otc Drug
    Labeler Name:
    S.s.s. Company
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    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):
  • PRAMOXINE HYDROCHLORIDE 1 g/100mL
    • 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:
    08-31-1995
    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 12258-223-05?

    The NDC Packaged Code 12258-223-05 is assigned to a package of 1 bottle in 1 carton / 15 ml in 1 bottle of Curasore, a human over the counter drug labeled by S.s.s. Company. The product's dosage form is liquid and is administered via topical form.

    Is NDC 12258-223 included in the NDC Directory?

    Yes, Curasore with product code 12258-223 is active and included in the NDC Directory. The product was first marketed by S.s.s. Company on August 31, 1995 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 12258-223-05?

    The 11-digit format is 12258022305. 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
    5-3-212258-223-055-4-212258-0223-05