NDC 43742-1695 Respiratory Plus
Ribes Nigrum,Viburnum Opulus,Quebracho,Blatta Orientalis,Pothos Foetidus,Cinnamic - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43742-1695?
What are the uses for Respiratory Plus?
What are Respiratory Plus Active Ingredients?
- ARSENIC TRIIODIDE 8 [hp_X]/mL
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK 5 [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 MONOHYDRATE 6 [hp_X]/mL
- 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.
- 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 Respiratory 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)
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK (UNII: 52B1340190)
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK (UNII: 52B1340190) (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 MONOHYDRATE (UNII: 48339473OT)
- 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 Respiratory 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 Respiratory 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.
[11] 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.
[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".