NDC 43406-0223 Allergy South East Mix
Birch Mix,Common Mugwort,English Plantain,Maple Mix,Pigweed Mix,Pine Mix,Ragweed Mix,Red - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43406 - Natural Creations, Inc
- 43406-0223 - Allergy South East Mix
Product Packages
NDC Code 43406-0223-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43406-0223?
What are the uses for Allergy South East Mix?
What are Allergy South East Mix Active Ingredients?
- ACER NEGUNDO WOOD 6 [hp_X]/mL
- AMBROSIA CONFERTIFLORA WHOLE 6 [hp_X]/mL
- ARTEMISIA VULGARIS POLLEN 6 [hp_X]/mL
- BETULA PENDULA WHOLE 6 [hp_X]/mL
- CHENOPODIUM ALBUM WHOLE 6 [hp_X]/mL
- JUNIPERUS VIRGINIANA POLLEN 6 [hp_X]/mL
- MORUS RUBRA WHOLE 6 [hp_X]/mL
- PINUS SPP. WHOLE 6 [hp_X]/mL
- PLANTAGO LANCEOLATA POLLEN 6 [hp_X]/mL
- POPULUS ALBA WHOLE 6 [hp_X]/mL
- QUERCUS SPP. WHOLE 6 [hp_X]/mL
- RUMEX ACETOSELLA WHOLE 6 [hp_X]/mL
Which are Allergy South East Mix UNII Codes?
The UNII codes for the active ingredients in this product are:
- BETULA PENDULA WHOLE (UNII: 18J93016IT)
- BETULA PENDULA WHOLE (UNII: 18J93016IT) (Active Moiety)
- ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
- ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (Active Moiety)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
- ACER NEGUNDO WOOD (UNII: MGR889C1JE)
- ACER NEGUNDO WOOD (UNII: MGR889C1JE) (Active Moiety)
- QUERCUS SPP. WHOLE (UNII: MF4E5I2OUQ)
- QUERCUS SPP. WHOLE (UNII: MF4E5I2OUQ) (Active Moiety)
- CHENOPODIUM ALBUM WHOLE (UNII: O417YBE692)
- CHENOPODIUM ALBUM WHOLE (UNII: O417YBE692) (Active Moiety)
- PINUS SPP. WHOLE (UNII: NT5UBA3P7Z)
- PINUS SPP. WHOLE (UNII: NT5UBA3P7Z) (Active Moiety)
- AMBROSIA CONFERTIFLORA WHOLE (UNII: IM2D62E64F)
- AMBROSIA CONFERTIFLORA WHOLE (UNII: IM2D62E64F) (Active Moiety)
- JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G)
- JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (Active Moiety)
- MORUS RUBRA WHOLE (UNII: NIJ0Z7376A)
- MORUS RUBRA WHOLE (UNII: NIJ0Z7376A) (Active Moiety)
- RUMEX ACETOSELLA WHOLE (UNII: D4MF746504)
- RUMEX ACETOSELLA WHOLE (UNII: D4MF746504) (Active Moiety)
- POPULUS ALBA WHOLE (UNII: Y05EGY83Y4)
- POPULUS ALBA WHOLE (UNII: Y05EGY83Y4) (Active Moiety)
Which are Allergy South East Mix 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:
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Allergy South East Mix?
* 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".