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  5. NDC Package Code: 66096-747-03 Acne Relief Gel

NDC Package 66096-747-03 Acne Relief Gel

Calendula Officinalis,Chamomilla,Berberis Aquafolium,Hamamelis,Hepar Sulph. Calc. ,Sulphur - 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:
66096-747-03
Package Description:
50 g in 1 TUBE
Product Code:
66096-747
Proprietary Name:
Acne Relief Gel
Non-Proprietary Name:
Calendula Officinalis, Chamomilla, Berberis Aquafolium, Hamamelis, Hepar Sulph. Calc. , Sulphur
Substance Name:
Berberis Aquifolium Root Bark; Calcium Sulfide; Calendula Officinalis Flowering Top; Hamamelis Virginiana Root Bark/stem Bark; Matricaria Chamomilla; Sulfur
11-Digit NDC Billing Format:
66096074703
Product Type:
Human Otc Drug
Labeler Name:
Ohm Pharma Inc.
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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):
  • BERBERIS AQUIFOLIUM ROOT BARK 2 [hp_X]/50g
  • CALCIUM SULFIDE 6 [hp_X]/50g
  • CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/50g
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 2 [hp_X]/50g
  • MATRICARIA CHAMOMILLA 1 [hp_X]/50g
  • SULFUR 6 [hp_X]/50g
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    11-29-2018
    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 66096-747-03?

    The NDC Packaged Code 66096-747-03 is assigned to a package of 50 g in 1 tube of Acne Relief Gel, a human over the counter drug labeled by Ohm Pharma Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 66096-747 included in the NDC Directory?

    Yes, Acne Relief Gel with product code 66096-747 is active and included in the NDC Directory. The product was first marketed by Ohm Pharma Inc. on November 29, 2018 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 66096-747-03?

    The 11-digit format is 66096074703. 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
    5-3-266096-747-035-4-266096-0747-03