NDC Package 12022-032-00 Sulfur 8 Scalp Therapy Medicated Dandruff Control

Salicylic Acid Spray Topical - View Billable Units, 11-Digit Format, RxNorm

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:
12022-032-00
Package Description:
355 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Sulfur 8 Scalp Therapy Medicated Dandruff Control
Non-Proprietary Name:
Salicylic Acid
Substance Name:
Salicylic Acid
Usage Information:
This medication is used on the skin to treat common skin and foot (plantar) warts. Salicylic acid helps cause the wart to gradually peel off. This medication is also used to help remove corns and calluses. This product should not be used on the face or on moles, birthmarks, warts with hair growing from them, or genital/anal warts. Salicylic acid is a keratolytic. It belongs to the same class of drugs as aspirin (salicylates). It works by increasing the amount of moisture in the skin and dissolving the substance that causes the skin cells to stick together. This makes it easier to shed the skin cells. Warts are caused by a virus. Salicylic acid does not affect the virus.
11-Digit NDC Billing Format:
12022003200
NDC to RxNorm Crosswalk:
  • RxCUI: 1048903 - salicylic acid 2 % Topical Spray
  • RxCUI: 1048903 - salicylic acid 20 MG/ML Topical Spray
  • Product Type:
    Human Otc Drug
    Labeler Name:
    J. Strickland And Co.
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    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):
    Sample Package:
    No
    FDA Application Number:
    M032
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-01-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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.

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    Frequently Asked Questions

    What is NDC 12022-032-00?

    The NDC Packaged Code 12022-032-00 is assigned to a package of 355 ml in 1 bottle of Sulfur 8 Scalp Therapy Medicated Dandruff Control, a human over the counter drug labeled by J. Strickland And Co.. The product's dosage form is spray and is administered via topical form.

    Is NDC 12022-032 included in the NDC Directory?

    Yes, Sulfur 8 Scalp Therapy Medicated Dandruff Control with product code 12022-032 is active and included in the NDC Directory. The product was first marketed by J. Strickland And Co. on January 01, 2020 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 12022-032-00?

    The 11-digit format is 12022003200. 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
    5-3-212022-032-005-4-212022-0032-00