NDC 59469-102 Apo-stom
Antimony Trisulfide,Atropa Bella-donna Flowering Top,Colchicum Autumnale Bulb,Citrullus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59469 - Pekana Naturheilmittel Gmbh
- 59469-102 - Apo-stom
Product Packages
NDC Code 59469-102-10
Package Description: 1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 59469-102?
What are the uses for Apo-stom?
What are Apo-stom Active Ingredients?
- ACHILLEA MILLEFOLIUM FLOWERING TOP 2606 mg/50mL
- ANTIMONY TRISULFIDE 8 [hp_X]/50mL
- ATROPA BELLA-DONNA FLOWERING TOP 4 [hp_X]/50mL
- CITRULLUS COLOCYNTHIS FRUIT PULP 4 [hp_X]/50mL
- COLCHICUM AUTUMNALE BULB 6 [hp_X]/50mL
- ROBINIA PSEUDOACACIA BARK 6 [hp_X]/50mL
- SODIUM PHOSPHATE 4 [hp_X]/50mL
- STRYCHNOS NUX-VOMICA SEED 4 [hp_X]/50mL
Which are Apo-stom UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
- ATROPA BELLA-DONNA FLOWERING TOP (UNII: B26WXN5GZJ)
- ATROPA BELLA-DONNA FLOWERING TOP (UNII: B26WXN5GZJ) (Active Moiety)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- ROBINIA PSEUDOACACIA BARK (UNII: 7TPC058OWY)
- ROBINIA PSEUDOACACIA BARK (UNII: 7TPC058OWY) (Active Moiety)
- ACHILLEA MILLEFOLIUM FLOWERING TOP (UNII: 55862Q3XEU)
- ACHILLEA MILLEFOLIUM FLOWERING TOP (UNII: 55862Q3XEU) (Active Moiety)
Which are Apo-stom 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 Apo-stom?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
* 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".