NDC 43742-1529 Asthma Plus
Ribes Nigrum,Viburnum Opulus,Quebracho,Blatta Orientalis,Pothos Foetidus,Cinnamic - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1529 - Asthma Plus
Product Packages
NDC Code 43742-1529-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1529?
What are the uses for Asthma Plus?
What are Asthma Plus Active Ingredients?
- ARSENIC TRIIODIDE 8 [hp_X]/mL
- BLATTA ORIENTALIS 6 [hp_X]/mL
- CINNAMIC ACID 6 [hp_X]/mL
- COUMARIN 8 [hp_X]/mL
- DERMATOPHAGOIDES FARINAE 9 [hp_C]/mL - Species of American house dust mite, in the family PYROGLYPHIDAE.
- GALLIC ACID 6 [hp_X]/mL - A colorless or slightly yellow crystalline compound obtained from nutgalls. It is used in photography, pharmaceuticals, and as an analytical reagent.
- INDOLE 6 [hp_X]/mL
- MALVIN 12 [hp_C]/mL
- NAPHTHALENE 8 [hp_X]/mL
- OXYGEN 12 [hp_X]/mL - An element with atomic symbol O, atomic number 8, and atomic weight [15.99903; 15.99977]. It is the most abundant element on earth and essential for respiration.
- QUEBRACHO BARK 5 [hp_X]/mL
- QUERCETIN 6 [hp_X]/mL - A flavonol widely distributed in plants. It is an antioxidant, like many other phenolic heterocyclic compounds. Glycosylated forms include RUTIN and quercetrin.
- RIBES NIGRUM LEAF 3 [hp_X]/mL
- RUTIN 6 [hp_X]/mL - A flavonol glycoside found in many plants, including BUCKWHEAT; TOBACCO; FORSYTHIA; HYDRANGEA; VIOLA, etc. It has been used therapeutically to decrease capillary fragility.
- SYMPLOCARPUS FOETIDUS ROOT 6 [hp_X]/mL
- VIBURNUM OPULUS BARK 3 [hp_X]/mL
Which are Asthma Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- RIBES NIGRUM LEAF (UNII: Z46FSZ2M25)
- RIBES NIGRUM LEAF (UNII: Z46FSZ2M25) (Active Moiety)
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805)
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805) (Active Moiety)
- QUEBRACHO BARK (UNII: HST8772GTZ)
- QUEBRACHO BARK (UNII: HST8772GTZ) (Active Moiety)
- BLATTA ORIENTALIS (UNII: 535787266D)
- BLATTA ORIENTALIS (UNII: 535787266D) (Active Moiety)
- SYMPLOCARPUS FOETIDUS ROOT (UNII: R88254608W)
- SYMPLOCARPUS FOETIDUS ROOT (UNII: R88254608W) (Active Moiety)
- CINNAMIC ACID (UNII: U14A832J8D)
- CINNAMIC ACID (UNII: U14A832J8D) (Active Moiety)
- GALLIC ACID (UNII: 632XD903SP)
- GALLIC ACID (UNII: 632XD903SP) (Active Moiety)
- INDOLE (UNII: 8724FJW4M5)
- INDOLE (UNII: 8724FJW4M5) (Active Moiety)
- QUERCETIN (UNII: 9IKM0I5T1E)
- QUERCETIN (UNII: 9IKM0I5T1E) (Active Moiety)
- RUTIN (UNII: 5G06TVY3R7)
- RUTIN (UNII: 5G06TVY3R7) (Active Moiety)
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- NAPHTHALENE (UNII: 2166IN72UN)
- NAPHTHALENE (UNII: 2166IN72UN) (Active Moiety)
- COUMARIN (UNII: A4VZ22K1WT)
- COUMARIN (UNII: A4VZ22K1WT) (Active Moiety)
- OXYGEN (UNII: S88TT14065)
- OXYGEN (UNII: S88TT14065) (Active Moiety)
- DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q)
- DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q) (Active Moiety)
- MALVIN (UNII: I9I120531L)
- MALVIN (UNII: I9I120531L) (Active Moiety)
Which are Asthma Plus 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 Asthma Plus?
- Allergens - [CS]
- Allergens - [CS]
- Antigens, Dermatophagoides - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Insect Proteins - [CS]
- Non-Standardized Insect Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Standardized Insect Allergenic Extract - [EPC] (Established Pharmacologic Class)
* 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".