NDC Package 71781-0003-1 Homeoplex D

Glycerinum,Phytolacca Decandra,Taraxacum Officinale,Arsenicum Album,Nitricum Acidum,Nux - 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:
71781-0003-1
Package Description:
60 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Homeoplex D
Non-Proprietary Name:
Glycerinum, Phytolacca Decandra, Taraxacum Officinale, Arsenicum Album, Nitricum Acidum, Nux Vomica, Petroleum, Phosphoricum Acidum, Phosphorus, Acetylsalicylicum Acidum, Glonoinum, Insulinum (suis), Lithium Carbonicum, Thyroidinum (suis), Salicylicum Acidum, Adrenocorticotrophin, Cortisone Aceticum, Eugenol, Stearyl Alcohol, Xylitol, Folliculinum, Benzoicum Acidum, Chlorinum, Potassium Sorbate, Sorbitol, Resorcinum, Benzyl Alcohol, Lacticum Acidum, Isopropyl Palmitate, Boricum Acidum, Aceticum Acidum,
Substance Name:
Acetic Acid; Arsenic Trioxide; Aspirin; Benzoic Acid; Benzyl Alcohol; Boric Acid; Chlorine; Corticotropin; Cortisone Acetate; Estrone; Eugenol; Glycerin; Insulin Pork; Isopropyl Palmitate; Kerosene; Lactic Acid, Dl-; Lead; Lithium Carbonate; Nitric Acid; Nitroglycerin; Petrolatum; Phenylbutazone; Phosphoric Acid; Phosphorus; Phytolacca Americana Root; Potassium Sorbate; Resorcinol; Salicylic Acid; Sorbitol; Stearyl Alcohol; Strychnos Nux-vomica Seed; Sus Scrofa Thyroid; Taraxacum Officinale; Xylitol
Usage Information:
For support of body's elimination systems. For support of body's elimination systems.
11-Digit NDC Billing Format:
71781000301
Product Type:
Human Otc Drug
Labeler Name:
Supplement Clinic, Llc.
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:
    11-01-2017
    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 71781-0003-1?

    The NDC Packaged Code 71781-0003-1 is assigned to a package of 60 ml in 1 bottle, dropper of Homeoplex D, a human over the counter drug labeled by Supplement Clinic, Llc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 71781-0003 included in the NDC Directory?

    Yes, Homeoplex D with product code 71781-0003 is active and included in the NDC Directory. The product was first marketed by Supplement Clinic, Llc. on November 01, 2017 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 71781-0003-1?

    The 11-digit format is 71781000301. 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
    5-4-171781-0003-15-4-271781-0003-01