NDC 48951-8086 Pulmo Echinacea
Pellet Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 48951 - Uriel Pharmacy Inc.
- 48951-8086 - Pulmo Echinacea
Product Characteristics
Product Packages
NDC Code 48951-8086-2
Package Description: 1350 PELLET in 1 BOTTLE, GLASS
Product Details
What is NDC 48951-8086?
What are the uses for Pulmo Echinacea?
What are Pulmo Echinacea Active Ingredients?
- ASTRAGALUS PROPINQUUS ROOT 3 [hp_X]/1
- ATROPA BELLADONNA 3 [hp_X]/1 - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- ECHINACEA ANGUSTIFOLIA 2 [hp_X]/1 - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- FERROSOFERRIC PHOSPHATE 6 [hp_X]/1
- LACHESIS MUTA VENOM 12 [hp_X]/1
- SILVER 30 [hp_X]/1 - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
- SUS SCROFA LUNG 17 [hp_X]/1
- TARAXACUM PALUSTRE ROOT 4 [hp_X]/1
Which are Pulmo Echinacea UNII Codes?
The UNII codes for the active ingredients in this product are:
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C)
- TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- SUS SCROFA LUNG (UNII: 7GL3G1COB3)
- SUS SCROFA LUNG (UNII: 7GL3G1COB3) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
Which are Pulmo Echinacea 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:
- SUCROSE (UNII: C151H8M554)
- LACTOSE (UNII: J2B2A4N98G)
* 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".