NDC 43742-1606 Reflux

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

NDC Product Code 43742-1606

NDC CODE: 43742-1606

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: Adenosinum Triphosphoricum Dinatrum, Nadidum, Argentum Nitricum, Robinia Pseudoacacia, Sulphur, Origanum Vulgare, Duodenum (suis), Esophagus (suis), Funiculus Umbilicalis Suis, Stomach (suis), Nux Vomica, Coumarinum, Pancreatinum, Muriaticum Acidum, Citricum Acidum, Formicum Acidum, Sarcolacticum Acidum, Coenzyme A, 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.

NDC 43742-1606-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Reflux with NDC 43742-1606 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Reflux is adenosinum triphosphoricum dinatrum, nadidum, argentum nitricum, robinia pseudoacacia, sulphur, origanum vulgare, duodenum (suis), esophagus (suis), funiculus umbilicalis suis, stomach (suis), nux vomica, coumarinum, pancreatinum, muriaticum acidum, citricum acidum, formicum acidum, sarcolacticum acidum, coenzyme a, 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.

  • ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_X]/mL
  • NADIDE 6 [hp_X]/mL
  • SILVER NITRATE 6 [hp_X]/mL
  • ROBINIA PSEUDOACACIA BARK 6 [hp_X]/mL
  • SULFUR 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
  • STRYCHNOS NUX-VOMICA SEED 8 [hp_X]/mL
  • COUMARIN 8 [hp_X]/mL
  • PANCRELIPASE 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
  • COENZYME A 8 [hp_C]/mL
  • PROTEUS MORGANII 30 [hp_C]/mL

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: 11-04-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

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’.

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Reflux Product Label Images