NDC 43742-1259 Bio Placenta Phase
Aesculus Hippocastanum,Sarcolacticum Acidum,Cuprum Sulphuricum,Melilotus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1259 - Bio Placenta Phase
Product Packages
NDC Code 43742-1259-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1259?
What are the uses for Bio Placenta Phase?
What are Bio Placenta Phase Active Ingredients?
- ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING 6 [hp_C]/mL
- BARIUM CARBONATE 13 [hp_X]/mL
- CLAVICEPS PURPUREA SCLEROTIUM 8 [hp_X]/mL
- CUPRIC SULFATE 6 [hp_X]/mL
- HORSE CHESTNUT 4 [hp_X]/mL - A plant genus of the family HIPPOCASTANACEAE (or SAPINDACEAE by some) that contains antimicrobial protein 1 and escin. A. hippocastanum is used in folk medicine for treating chronic venous insufficiency.
- LACTIC ACID, L- 4 [hp_X]/mL
- LEAD IODIDE 18 [hp_X]/mL
- MELILOTUS OFFICINALIS TOP 6 [hp_X]/mL
- PRASTERONE 6 [hp_X]/mL
- PROTEUS VULGARIS 30 [hp_C]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that occurs in soil, fecal matter, and sewage. It is an opportunistic pathogen and causes cystitis and pyelonephritis.
- 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.
- 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.
- SODIUM PYRUVATE 8 [hp_X]/mL
- SOLANUM NIGRUM WHOLE 6 [hp_X]/mL
- STROPHANTHUS HISPIDUS SEED 6 [hp_X]/mL
- SUS SCROFA ARTERY 8 [hp_X]/mL
- SUS SCROFA PLACENTA 6 [hp_X]/mL
- SUS SCROFA UMBILICAL CORD 10 [hp_X]/mL
- SUS SCROFA VEIN 8 [hp_X]/mL
- TOBACCO LEAF 10 [hp_X]/mL
- VIPERA BERUS VENOM 10 [hp_X]/mL
Which are Bio Placenta Phase UNII Codes?
The UNII codes for the active ingredients in this product are:
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- CUPRIC SULFATE (UNII: LRX7AJ16DT)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
- MELILOTUS OFFICINALIS TOP (UNII: GM6P02J2DX)
- MELILOTUS OFFICINALIS TOP (UNII: GM6P02J2DX) (Active Moiety)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8) (Active Moiety)
- SOLANUM NIGRUM WHOLE (UNII: 0FMD6WV47M)
- SOLANUM NIGRUM WHOLE (UNII: 0FMD6WV47M) (Active Moiety)
- STROPHANTHUS HISPIDUS SEED (UNII: MO892VI77K)
- STROPHANTHUS HISPIDUS SEED (UNII: MO892VI77K) (Active Moiety)
- PRASTERONE (UNII: 459AG36T1B)
- PRASTERONE (UNII: 459AG36T1B) (Active Moiety)
- QUERCETIN (UNII: 9IKM0I5T1E)
- QUERCETIN (UNII: 9IKM0I5T1E) (Active Moiety)
- RUTIN (UNII: 5G06TVY3R7)
- RUTIN (UNII: 5G06TVY3R7) (Active Moiety)
- SODIUM PYRUVATE (UNII: POD38AIF08)
- PYRUVIC ACID (UNII: 8558G7RUTR) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
- SUS SCROFA VEIN (UNII: 2510RH3I89)
- SUS SCROFA VEIN (UNII: 2510RH3I89) (Active Moiety)
- SUS SCROFA ARTERY (UNII: 63O327782Q)
- SUS SCROFA ARTERY (UNII: 63O327782Q) (Active Moiety)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (Active Moiety)
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
- VIPERA BERUS VENOM (UNII: 0ORO6NCA4M)
- VIPERA BERUS VENOM (UNII: 0ORO6NCA4M) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- LEAD IODIDE (UNII: OTL90F2GLT)
- LEAD IODIDE (UNII: OTL90F2GLT) (Active Moiety)
- ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING (UNII: 0II1G590JE)
- ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING (UNII: 0II1G590JE) (Active Moiety)
- PROTEUS VULGARIS (UNII: 11T9HCO30O)
- PROTEUS VULGARIS (UNII: 11T9HCO30O) (Active Moiety)
Which are Bio Placenta Phase 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 Bio Placenta Phase?
* 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".