NDC 63479-0406 D06 Bldr-drn
Apis Mellifica,Argentum Nitricum,Badiaga,Belladonna,Cantharis,Causticum,Chimaphila - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 63479-0406?
What are the uses for D06 Bldr-drn?
What are D06 Bldr-drn Active Ingredients?
- APIS MELLIFERA 6 [hp_X]/mL
- ARCTOSTAPHYLOS UVA-URSI LEAF 1 [hp_X]/mL
- ATROPA BELLADONNA 10 [hp_X]/mL - 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.
- CAUSTICUM 8 [hp_X]/mL
- CHIMAPHILA UMBELLATA 2 [hp_X]/mL
- CITRULLUS COLOCYNTHIS FRUIT PULP 8 [hp_X]/mL
- CUCURBITA PEPO FLOWER 3 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 1 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- EQUISETUM HYEMALE 6 [hp_X]/mL
- ERYNGIUM YUCCIFOLIUM ROOT 2 [hp_X]/mL
- FERROSOFERRIC PHOSPHATE 10 [hp_X]/mL
- LYTTA VESICATORIA 12 [hp_X]/mL
- MACROPIPER METHYSTICUM ROOT 2 [hp_X]/mL
- MITCHELLA REPENS 1 [hp_X]/mL
- PETROSELINUM CRISPUM 3 [hp_X]/mL - A plant genus of the family APIACEAE used for flavoring food.
- PIPER CUBEBA FRUIT 3 [hp_X]/mL
- POPULUS TREMULOIDES BARK 2 [hp_X]/mL
- SANDALWOOD OIL 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.
- SMILAX ORNATA ROOT 6 [hp_X]/mL
- SPONGILLA LACUSTRIS 8 [hp_X]/mL
- TURPENTINE OIL 8 [hp_X]/mL
- WATERMELON SEED 3 [hp_X]/mL
Which are D06 Bldr-drn UNII Codes?
The UNII codes for the active ingredients in this product are:
- SANDALWOOD OIL (UNII: X7X01WMQ5F)
- SANDALWOOD OIL (UNII: X7X01WMQ5F) (Active Moiety)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (Active Moiety)
- CHIMAPHILA UMBELLATA (UNII: WCK21A9W9J)
- CHIMAPHILA UMBELLATA (UNII: WCK21A9W9J) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- SPONGILLA LACUSTRIS (UNII: 6SZ0G98BHM)
- SPONGILLA LACUSTRIS (UNII: 6SZ0G98BHM) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- TURPENTINE OIL (UNII: C5H0QJ6V7F)
- TURPENTINE OIL (UNII: C5H0QJ6V7F) (Active Moiety)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG) (Active Moiety)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
- WATERMELON SEED (UNII: N364973Y9Q)
- WATERMELON SEED (UNII: N364973Y9Q) (Active Moiety)
- CUCURBITA PEPO FLOWER (UNII: 413MGP37HQ)
- CUCURBITA PEPO FLOWER (UNII: 413MGP37HQ) (Active Moiety)
- POPULUS TREMULOIDES BARK (UNII: 5543O0CEID)
- POPULUS TREMULOIDES BARK (UNII: 5543O0CEID) (Active Moiety)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- PIPER CUBEBA FRUIT (UNII: Z99L7429MA)
- PIPER CUBEBA FRUIT (UNII: Z99L7429MA) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- EQUISETUM HYEMALE (UNII: 59677RXH25)
- EQUISETUM HYEMALE (UNII: 59677RXH25) (Active Moiety)
- MITCHELLA REPENS (UNII: 1H23589PLJ)
- MITCHELLA REPENS (UNII: 1H23589PLJ) (Active Moiety)
- ERYNGIUM YUCCIFOLIUM ROOT (UNII: 612HZ21596)
- ERYNGIUM YUCCIFOLIUM ROOT (UNII: 612HZ21596) (Active Moiety)
- MACROPIPER METHYSTICUM ROOT (UNII: BOW48C81XP)
- MACROPIPER METHYSTICUM ROOT (UNII: BOW48C81XP) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
Which are D06 Bldr-drn 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for D06 Bldr-drn?
* 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".