NDC 43742-0739 Reflux

Acetyl Coenzyme A, Adenosinum Triphosphoricum Dinatrum, Nadidum, Coumarinum, Argentum Nitricum, Ipecacuanha, Robinia Pseudoacacia, Sulphur, Nux Vomica, Origanum Vulgare, Duodenum (suis), Esophagus (suis), Funiculus Umbilicalis Suis, Stomach (suis), Erythraea Centaurium, Pepsinum, Muriaticum Acidum, Citricum Acidum, Formicum Acidum, Sarcolacticum Acidum, Proteus (morgani)

NDC Product Code 43742-0739

NDC Code: 43742-0739

Proprietary Name: Reflux What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Acetyl Coenzyme A, Adenosinum Triphosphoricum Dinatrum, Nadidum, Coumarinum, Argentum Nitricum, Ipecacuanha, Robinia Pseudoacacia, Sulphur, Nux Vomica, Origanum Vulgare, Duodenum (suis), Esophagus (suis), Funiculus Umbilicalis Suis, Stomach (suis), Erythraea Centaurium, Pepsinum, Muriaticum Acidum, Citricum Acidum, Formicum Acidum, Sarcolacticum Acidum, Proteus (morgani) What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.
    • 43742-0739 - Reflux

NDC 43742-0739-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Reflux with NDC 43742-0739 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Reflux is acetyl coenzyme a, adenosinum triphosphoricum dinatrum, nadidum, coumarinum, argentum nitricum, ipecacuanha, robinia pseudoacacia, sulphur, nux vomica, origanum vulgare, duodenum (suis), esophagus (suis), funiculus umbilicalis suis, stomach (suis), erythraea centaurium, pepsinum, muriaticum acidum, citricum acidum, formicum acidum, sarcolacticum acidum, proteus (morgani). The product's dosage form is liquid and is administered via oral form.

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.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Reflux Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ACETYL COENZYME A 6 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_X]/mL
  • NADIDE 6 [hp_X]/mL
  • COUMARIN 6 [hp_X]/mL
  • SILVER NITRATE 6 [hp_X]/mL
  • IPECAC 6 [hp_X]/mL
  • ROBINIA PSEUDOACACIA BARK 6 [hp_X]/mL
  • SULFUR 6 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/mL
  • OREGANO 6 [hp_X]/mL
  • SUS SCROFA DUODENUM 8 [hp_X]/mL
  • SUS SCROFA ESOPHAGUS 8 [hp_X]/mL
  • SUS SCROFA UMBILICAL CORD 8 [hp_X]/mL
  • SUS SCROFA STOMACH 8 [hp_X]/mL
  • CENTAURIUM ERYTHRAEA 10 [hp_X]/mL
  • PEPSIN 12 [hp_X]/mL
  • HYDROCHLORIC ACID 6 [hp_C]/mL
  • ANHYDROUS CITRIC ACID 6 [hp_C]/mL
  • FORMIC ACID 6 [hp_C]/mL
  • LACTIC ACID, L- 6 [hp_C]/mL
  • PROTEUS MORGANII 30 [hp_C]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 04-28-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 08-14-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Reflux Product Label Images

Reflux Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Acetyl Coenzyme A 6X, 8X, Adenosinum Triphosphoricum Dinatrum 6X, 8X, Nadidum 6X, 8X, Coumarinum 6X, 8X, 10X, 30X, 200X, Argentum Nitricum 6X, 10X, Ipecacuanha 6X, 10X, Robinia Pseudoacacia 6X, 10X, Sulphur 6X, 10X, Nux Vomica 6X, 10X, 30X, Origanum Vulgare 6X, 10X, 30X, Duodenum (Suis) 8X, Esophagus (Suis) 8X, Funiculus Umbilicalis Suis 8X, Stomach (Suis) 8X, Erythraea Centaurium 10X, 30X, Pepsinum 12X, Muriaticum Acidum 6C, 12C, 30C, 200C, Citricum Acidum 6C, 12C, 30C, 200C, Formicum Acidum 6C, 12C, 30C, 200C, Sarcolacticum Acidum 6C, 12C, 30C, 200C, Proteus (Morgani) 30C.

Homeopathic Indications:

For temporary relief of symptoms related to heartburn and esophageal reflux.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to heartburn and esophageal reflux.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

Directions:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol.

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070    www.desbio.com

Package Label Display:

DESBIONDC 43742-0739-1HOMEOPATHICREFLUX1 FL OZ (30 ml)

* Please review the disclaimer below.

Previous Code
43742-0737
Next Code
43742-0740