NDC Package 43742-1493-1 Bio Cytotox Phase

Podophyllum Peltatum,Ascorbicum Acidum,Galium Aparine,Hydrastis - 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:
43742-1493-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Bio Cytotox Phase
Non-Proprietary Name:
Podophyllum Peltatum, Ascorbicum Acidum, Galium Aparine, Hydrastis Canadensis, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Colchicum Autumnale, Conium Maculatum, Natrum Oxalaceticum, Sulphur, Vaccinium Myrtillus, Norepinephrine, Acetylsalicylicum Acidum, Adenosinum Triphosphoricum Dinatrum, Anthrachinonum, Histaminum Hydrochloricum, Magnesium Gluconicum Dihydricum, Nadidum, Naphthochinonum, Pantothenic Acid, Ubidecarenonum,
Substance Name:
Adenosine Triphosphate Disodium; Anthraquinone; Ascorbic Acid; Aspirin; Bilberry; Colchicum Autumnale Bulb; Conium Maculatum Flowering Top; Galium Aparine; Goldenseal; Histamine Dihydrochloride; Hydroquinone; Lactic Acid, L-; Magnesium Gluconate; Manganese Phosphate, Dibasic; Nadide; Naphthoquine; Niacinamide; Norepinephrine Bitartrate; Pantothenic Acid; Podophyllum; Pyridoxine Hydrochloride; Riboflavin; Salmonella Enterica Subsp. Enterica Serovar Enteritidis; Sodium Diethyl Oxalacetate; Sulfur; Thiamine Hydrochloride; Thioctic Acid; Ubidecarenone
Usage Information:
For the temporary relief of symptoms of fatigue, slowed metabolism, and weakened constitution.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms of fatigue, slowed metabolism, and weakened constitution.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742149301
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.
  • Pharmacologic Class(es):
  • Analogs/Derivatives - [Chemical/Ingredient]
  • Anti-Inflammatory Agents, Non-Steroidal - [CS]
  • Ascorbic Acid - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Catecholamine - [EPC] (Established Pharmacologic Class)
  • Catecholamines - [CS]
  • Cyclooxygenase Inhibitors - [MoA] (Mechanism of Action)
  • Decreased Platelet Aggregation - [PE] (Physiologic Effect)
  • Decreased Prostaglandin Production - [PE] (Physiologic Effect)
  • Depigmenting Activity - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Melanin Synthesis Inhibitor - [EPC] (Established Pharmacologic Class)
  • Melanin Synthesis Inhibitors - [MoA] (Mechanism of Action)
  • Nonsteroidal Anti-inflammatory Drug - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • Platelet Aggregation Inhibitor - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
  • Vitamin B 6 - [Chemical/Ingredient]
  • Vitamin B6 Analog - [EPC] (Established Pharmacologic Class)
  • Vitamin C - [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:
    07-09-2019
    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 43742-1493-1?

    The NDC Packaged Code 43742-1493-1 is assigned to a package of 30 ml in 1 bottle, dropper of Bio Cytotox Phase, 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 43742-1493 included in the NDC Directory?

    Yes, Bio Cytotox Phase with product code 43742-1493 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on July 09, 2019 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 43742-1493-1?

    The 11-digit format is 43742149301. 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
    5-4-143742-1493-15-4-243742-1493-01