NDC Package 71953-0001-1 Supreme

Abrotanum,Anacardium Orientale,Arsenicum Album,Baryta Muriatica,Helleborus Niger,Ignatia - 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:
71953-0001-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Supreme
Non-Proprietary Name:
Abrotanum, Anacardium Orientale, Arsenicum Album, Baryta Muriatica, Helleborus Niger, Ignatia Amara, Lycopodium Clavatum, Nicotinamidum, Secale Cornutum, Thymus (bovine), Thyroidinum (bovine), Calcarea Carbonica, Calcarea Phosphorica, Hypothalamus Suis, Pituitarum Posterium (bovine), Silicea
Substance Name:
Anacardium Occidentale Fruit; Arsenic Trioxide; Artemisia Abrotanum Flowering Top; Barium Chloride Dihydrate; Bos Taurus Pituitary Gland, Posterior; Bos Taurus Thymus; Claviceps Purpurea Sclerotium; Helleborus Niger Root; Lycopodium Clavatum Spore; Niacinamide; Oyster Shell Calcium Carbonate, Crude; Silicon Dioxide; Strychnos Ignatii Seed; Sus Scrofa Hypothalamus; Thyroid, Bovine; Tribasic Calcium Phosphate
Usage Information:
Helps improve diencephalic banking of fat for consumption by the body. Helps improve diencephalic banking of fat for consumption by the body.
11-Digit NDC Billing Format:
71953000101
Product Type:
Human Otc Drug
Labeler Name:
Bouari Group, Llc Dba Weight Loss Company, The
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):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    05-17-2018
    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 71953-0001-1?

    The NDC Packaged Code 71953-0001-1 is assigned to a package of 30 ml in 1 bottle, dropper of Supreme, a human over the counter drug labeled by Bouari Group, Llc Dba Weight Loss Company, The. The product's dosage form is liquid and is administered via oral form.

    Is NDC 71953-0001 included in the NDC Directory?

    Yes, Supreme with product code 71953-0001 is active and included in the NDC Directory. The product was first marketed by Bouari Group, Llc Dba Weight Loss Company, The on May 17, 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 71953-0001-1?

    The 11-digit format is 71953000101. 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
    5-4-171953-0001-15-4-271953-0001-01