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  5. NDC Package Code: 43742-1681-1 Amoe Combination

NDC Package 43742-1681-1 Amoe Combination

Baptisia Tinctoria,Cajuputum,Capsicum Annuum,Fragaria Vesca,Hamamelis Virginiana,Quassia - 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:
43742-1681-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-1681
Proprietary Name:
Amoe Combination
Non-Proprietary Name:
Baptisia Tinctoria, Cajuputum, Capsicum Annuum, Fragaria Vesca, Hamamelis Virginiana, Quassia (amara), Senna (cassia Angustifolia), Hydrastis Canadensis, Hepar Suis, Pancreas Suis, Spleen (suis), Cinchona Officinalis, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Selenium Metallicum, Blastocystis Hominis, Cryptosporidium Parvum, Giardia Lamblia, Entamoeba Histolytica, Brugia Malayi
Substance Name:
Baptisia Tinctoria Root; Blastocystis Hominis; Brugia Malayi; Cajuput Oil; Capsicum; Cinchona Officinalis Bark; Cryptosporidium Parvum; Entamoeba Histolytica; Fragaria Vesca Fruit; Giardia Lamblia; Goldenseal; Hamamelis Virginiana Root Bark/stem Bark; Iridium; Lycopodium Clavatum Spore; Nitric Acid; Pork Liver; Quassia Amara Wood; Selenium; Senna Leaf; Strychnos Nux-vomica Seed; Sus Scrofa Pancreas; Sus Scrofa Spleen
Usage Information:
For temporary relief of symptoms related to amoeba infestation including consequent weakness, fever, and stomach cramps.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to amoeba infestation including consequent weakness, fever, and stomach cramps.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742168101
Product Type:
Human Otc Drug
Labeler Name:
Deseret Biologicals, Inc.
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.
    • Active Ingredient(s):
  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
  • BLASTOCYSTIS HOMINIS 12 [hp_C]/mL
  • BRUGIA MALAYI 39 [hp_C]/mL
  • CAJUPUT OIL 3 [hp_X]/mL
  • CAPSICUM 3 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 12 [hp_X]/mL
  • CRYPTOSPORIDIUM PARVUM 12 [hp_C]/mL
  • ENTAMOEBA HISTOLYTICA 18 [hp_C]/mL
  • FRAGARIA VESCA FRUIT 3 [hp_X]/mL
  • GIARDIA LAMBLIA 12 [hp_C]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 3 [hp_X]/mL
  • IRIDIUM 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • PORK LIVER 8 [hp_X]/mL
  • QUASSIA AMARA WOOD 3 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL
  • SENNA LEAF 3 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • SUS SCROFA PANCREAS 8 [hp_X]/mL
  • SUS SCROFA SPLEEN 8 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
  • Vegetable Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    05-14-2021
    Listing Expiration Date:
    12-31-2025
    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 43742-1681-1?

    The NDC Packaged Code 43742-1681-1 is assigned to a package of 30 ml in 1 bottle, dropper of Amoe Combination, a human over the counter drug labeled by Deseret Biologicals, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43742-1681 included in the NDC Directory?

    Yes, Amoe Combination with product code 43742-1681 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on May 14, 2021 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 43742-1681-1?

    The 11-digit format is 43742168101. 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
    5-4-143742-1681-15-4-243742-1681-01