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  5. NDC Package Code: 43742-1250-1 Allermilk

NDC Package 43742-1250-1 Allermilk

Taraxacum Officinale,Hydrastis Canadensis,Apiolum,Benzoicum Acidum,Cholinum,Cinnamic - 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:
43742-1250-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-1250
Proprietary Name:
Allermilk
Non-Proprietary Name:
Taraxacum Officinale, Hydrastis Canadensis, Apiolum, Benzoicum Acidum, Cholinum, Cinnamic Acid, Eugenol, Folic Acid, Histaminum Hydrochloricum, L-asparagine, Menadione, Octopamine, Oophorinum (suis), Phenyl Isothiocyanate, Piperine, Progesterone, Quercetin, Rutin, Saccharum Lactis, Vanillylamine, Xanthine, Coumarinum, Folliculinum, Formalinum, Gaba (gamma-aminobutyric Acid).
Substance Name:
.gamma.-aminobutyric Acid; Apiole (parsley); Asparagine; Benzoic Acid; Choline Hydroxide; Cinnamic Acid; Coumarin; Estrone; Eugenol; Folic Acid; Formaldehyde; Goldenseal; Histamine Dihydrochloride; Lactose, Unspecified Form; Menadione; Octopamine Hydrochloride; Phenyl Isothiocyanate; Piperine; Progesterone; Quercetin; Rutin; Sus Scrofa Ovary; Taraxacum Officinale; Vanillylamine; Xanthine
Usage Information:
For the relief of symptoms related to sensitivity to milk or milk products including skin rash, hives, vomiting, bloating, cramping and occasional diarrhea.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the relief of symptoms related to sensitivity to milk or milk products including skin rash, hives, vomiting, bloating, cramping and occasional diarrhea.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742125001
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):
  • .GAMMA.-AMINOBUTYRIC ACID 8 [hp_X]/mL
  • APIOLE (PARSLEY) 6 [hp_X]/mL
  • ASPARAGINE 6 [hp_X]/mL
  • BENZOIC ACID 6 [hp_X]/mL
  • CHOLINE HYDROXIDE 6 [hp_X]/mL
  • CINNAMIC ACID 6 [hp_X]/mL
  • COUMARIN 8 [hp_X]/mL
  • ESTRONE 8 [hp_X]/mL
  • EUGENOL 6 [hp_X]/mL
  • FOLIC ACID 6 [hp_X]/mL
  • FORMALDEHYDE 8 [hp_X]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 6 [hp_X]/mL
  • LACTOSE, UNSPECIFIED FORM 6 [hp_X]/mL
  • MENADIONE 6 [hp_X]/mL
  • OCTOPAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • PHENYL ISOTHIOCYANATE 6 [hp_X]/mL
  • PIPERINE 6 [hp_X]/mL
  • PROGESTERONE 6 [hp_X]/mL
  • QUERCETIN 6 [hp_X]/mL
  • RUTIN 6 [hp_X]/mL
  • SUS SCROFA OVARY 6 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • VANILLYLAMINE 6 [hp_X]/mL
  • XANTHINE 6 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Ammonium Ion Binding Activity - [MoA] (Mechanism of Action)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Nitrogen Binding Agent - [EPC] (Established Pharmacologic Class)
  • Progesterone - [CS]
  • Progesterone - [EPC] (Established Pharmacologic Class)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    11-09-2018
    End Marketing Date:
    04-15-2024
    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 43742-1250-1?

    The NDC Packaged Code 43742-1250-1 is assigned to a package of 30 ml in 1 bottle, dropper of Allermilk, 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 43742-1250 included in the NDC Directory?

    Yes, Allermilk with product code 43742-1250 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on November 09, 2018.

    What is the 11-digit format for NDC 43742-1250-1?

    The 11-digit format is 43742125001. 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
    5-4-143742-1250-15-4-243742-1250-01