NDC 43742-1606 Reflux
Adenosinum Triphosphoricum Dinatrum,Nadidum,Argentum Nitricum,Robinia - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1606 - Reflux
Product Packages
NDC Code 43742-1606-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1606?
What are the uses for Reflux?
What are Reflux Active Ingredients?
- ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_X]/mL
- ANHYDROUS CITRIC ACID 6 [hp_C]/mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
- COENZYME A 8 [hp_C]/mL
- COUMARIN 8 [hp_X]/mL
- FORMIC ACID 6 [hp_C]/mL
- HYDROCHLORIC ACID 6 [hp_C]/mL - A strong corrosive acid that is commonly used as a laboratory reagent. It is formed by dissolving hydrogen chloride in water. GASTRIC ACID is the hydrochloric acid component of GASTRIC JUICE.
- LACTIC ACID, L- 6 [hp_C]/mL
- NADIDE 6 [hp_X]/mL
- OREGANO 6 [hp_X]/mL
- PANCRELIPASE 12 [hp_X]/mL - A preparation of hog pancreatic enzymes standardized for lipase content.
- PROTEUS MORGANII 30 [hp_C]/mL
- ROBINIA PSEUDOACACIA BARK 6 [hp_X]/mL
- SILVER NITRATE 6 [hp_X]/mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
- STRYCHNOS NUX-VOMICA SEED 8 [hp_X]/mL
- SULFUR 6 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
- SUS SCROFA DUODENUM 8 [hp_X]/mL
- SUS SCROFA ESOPHAGUS 8 [hp_X]/mL
- SUS SCROFA STOMACH 8 [hp_X]/mL
- SUS SCROFA UMBILICAL CORD 8 [hp_X]/mL
Which are Reflux UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- NADIDE (UNII: 0U46U6E8UK)
- NADIDE (UNII: 0U46U6E8UK) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- ROBINIA PSEUDOACACIA BARK (UNII: 7TPC058OWY)
- ROBINIA PSEUDOACACIA BARK (UNII: 7TPC058OWY) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- OREGANO (UNII: 0E5AT8T16U)
- OREGANO (UNII: 0E5AT8T16U) (Active Moiety)
- SUS SCROFA DUODENUM (UNII: P6J2SFT80O)
- SUS SCROFA DUODENUM (UNII: P6J2SFT80O) (Active Moiety)
- SUS SCROFA ESOPHAGUS (UNII: 81FZ7X4MWD)
- SUS SCROFA ESOPHAGUS (UNII: 81FZ7X4MWD) (Active Moiety)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (Active Moiety)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- COUMARIN (UNII: A4VZ22K1WT)
- COUMARIN (UNII: A4VZ22K1WT) (Active Moiety)
- PANCRELIPASE (UNII: FQ3DRG0N5K)
- PANCRELIPASE LIPASE (UNII: 8MYC33932O) (Active Moiety)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- HYDROCHLORIC ACID (UNII: QTT17582CB) (Active Moiety)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
- FORMIC ACID (UNII: 0YIW783RG1)
- FORMIC ACID (UNII: 0YIW783RG1) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- COENZYME A (UNII: SAA04E81UX)
- COENZYME A (UNII: SAA04E81UX) (Active Moiety)
- PROTEUS MORGANII (UNII: 56X6LID5ZY)
- PROTEUS MORGANII (UNII: 56X6LID5ZY) (Active Moiety)
Which are Reflux Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Reflux?
- Acidifying Activity - [MoA] (Mechanism of Action)
- Allergens - [CS]
- Anti-coagulant - [EPC] (Established Pharmacologic Class)
- Calcium Chelating Activity - [MoA] (Mechanism of Action)
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Decreased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [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]
* Please review the disclaimer below.
[1] 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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[10] 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.
[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".