NDC 43406-0114 Biting Insect Antigen
Apis Mellifera,Arnica Montana,Blatta Orientalis,Dieffenbachia Seguine,Cimex - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43406 - Natural Creations, Inc.
- 43406-0114 - Biting Insect Antigen
Product Packages
NDC Code 43406-0114-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43406-0114?
What are the uses for Biting Insect Antigen?
What are Biting Insect Antigen Active Ingredients?
- APIS MELLIFERA 12 [hp_C]/mL
- ARNICA MONTANA 30 [hp_C]/mL
- BLATTA ORIENTALIS 30 [hp_C]/mL
- CIMEX LECTULARIUS 30 [hp_C]/mL - Parasitic bugs of the family CIMICIDAE. Female bed bugs lay eggs in a sheltered locations such as in mattress seams. Adults and nymphal instars of Cimex feed on warm-blooded hosts. Cimex lectularius and Cimex hemipterus are implicated in human infestations.
- CULEX PIPIENS 30 [hp_C]/mL
- DELPHINIUM STAPHISAGRIA SEED 30 [hp_C]/mL
- DIEFFENBACHIA SEGUINE 12 [hp_C]/mL
- FORMICA RUFA 30 [hp_C]/mL
- HYPERICUM PERFORATUM 30 [hp_C]/mL
- LATRODECTUS MACTANS 30 [hp_C]/mL
- LEDUM PALUSTRE TWIG 30 [hp_C]/mL
- LOXOSCELES RECLUSA 30 [hp_C]/mL - A spider of the genus Loxosceles, found in the midwestern and other parts of the United States, which carries a hemolytic venom that produces local necrosis or ulceration.
- PEDICULUS HUMANUS VAR. CAPITIS 30 [hp_C]/mL
- PULEX IRRITANS 30 [hp_C]/mL
- VESPA CRABRO 30 [hp_C]/mL
Which are Biting Insect Antigen UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- BLATTA ORIENTALIS (UNII: 535787266D)
- BLATTA ORIENTALIS (UNII: 535787266D) (Active Moiety)
- DIEFFENBACHIA SEGUINE (UNII: 01800C6E6B)
- DIEFFENBACHIA SEGUINE (UNII: 01800C6E6B) (Active Moiety)
- CIMEX LECTULARIUS (UNII: W66P4K3SGW)
- CIMEX LECTULARIUS (UNII: W66P4K3SGW) (Active Moiety)
- CULEX PIPIENS (UNII: 45KA5D7541)
- CULEX PIPIENS (UNII: 45KA5D7541) (Active Moiety)
- FORMICA RUFA (UNII: 55H0W83JO5)
- FORMICA RUFA (UNII: 55H0W83JO5) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- LATRODECTUS MACTANS (UNII: XJJ7QA858R)
- LATRODECTUS MACTANS (UNII: XJJ7QA858R) (Active Moiety)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
- LOXOSCELES RECLUSA (UNII: 039G4OZ3G2)
- LOXOSCELES RECLUSA (UNII: 039G4OZ3G2) (Active Moiety)
- PEDICULUS HUMANUS VAR. CAPITIS (UNII: 29CA62712F)
- PEDICULUS HUMANUS VAR. CAPITIS (UNII: 29CA62712F) (Active Moiety)
- PULEX IRRITANS (UNII: L63DD62R8R)
- PULEX IRRITANS (UNII: L63DD62R8R) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- VESPA CRABRO (UNII: K3ALM8S49H)
- VESPA CRABRO (UNII: K3ALM8S49H) (Active Moiety)
Which are Biting Insect Antigen 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 Biting Insect Antigen?
- Allergens - [CS]
- Allergens - [CS]
- Bee Venoms - [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 Venom 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".