NDC 63479-1901 S01 Allerdrain
Aloe Socotrina,Berberis Vulgaris,Betula Verrucosa,Bryonia,Carduus Marianus,Echinacea - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 63479-1901?
What are the uses for S01 Allerdrain?
What are S01 Allerdrain Active Ingredients?
- ALOE 3 [hp_X]/mL - A plant genus of the family ASPHODELACEAE which is used medicinally. It contains anthraquinone glycosides such as aloin-emodin or aloe-emodin (EMODIN).
- BERBERIS VULGARIS ROOT BARK 1 [hp_X]/mL
- BETULA PENDULA LEAF 2 [hp_X]/mL
- BRYONIA ALBA ROOT 1 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 2 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- FRANGULA PURSHIANA BARK 1 [hp_X]/mL
- GINKGO 2 [hp_X]/mL
- HISTAMINE DIHYDROCHLORIDE 200 [hp_X]/mL - An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
- JUNIPERUS COMMUNIS STEM 2 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 4 [hp_X]/mL
- MILK THISTLE 2 [hp_X]/mL
- QUERCUS ROBUR FLOWER BUD 2 [hp_X]/mL
- RIBES NIGRUM FLOWER BUD 2 [hp_X]/mL
- ROSA CANINA LEAF 2 [hp_X]/mL
- ROSMARINUS OFFICINALIS FLOWERING TOP 2 [hp_X]/mL
- SCROPHULARIA NODOSA 2 [hp_X]/mL
- SENNA LEAF 2 [hp_X]/mL
- SOLIDAGO VIRGAUREA FLOWERING TOP 1 [hp_X]/mL
- TARAXACUM OFFICINALE 2 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
- TEA TREE OIL 12 [hp_X]/mL - Essential oil extracted from MELALEUCA ALTERNIFOLIA (tea tree). It is used as a topical antimicrobial due to the presence of terpineol.
- VACCINIUM VITIS-IDAEA LEAF 2 [hp_X]/mL
Which are S01 Allerdrain UNII Codes?
The UNII codes for the active ingredients in this product are:
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- FRANGULA PURSHIANA BARK (UNII: 4VBP01X99F)
- FRANGULA PURSHIANA BARK (UNII: 4VBP01X99F) (Active Moiety)
- QUERCUS ROBUR FLOWER BUD (UNII: VC5I578BE3)
- QUERCUS ROBUR FLOWER BUD (UNII: VC5I578BE3) (Active Moiety)
- RIBES NIGRUM FLOWER BUD (UNII: VYH9Y9BCCP)
- RIBES NIGRUM FLOWER BUD (UNII: VYH9Y9BCCP) (Active Moiety)
- ROSA CANINA LEAF (UNII: J3N2Z889QP)
- ROSA CANINA LEAF (UNII: J3N2Z889QP) (Active Moiety)
- MILK THISTLE (UNII: U946SH95EE)
- MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- TEA TREE OIL (UNII: VIF565UC2G)
- TEA TREE OIL (UNII: VIF565UC2G) (Active Moiety)
- ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79)
- ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) (Active Moiety)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- BETULA PENDULA LEAF (UNII: 5HW39H9KDH)
- BETULA PENDULA LEAF (UNII: 5HW39H9KDH) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- JUNIPERUS COMMUNIS STEM (UNII: HBU87MH6OY)
- JUNIPERUS COMMUNIS STEM (UNII: HBU87MH6OY) (Active Moiety)
- VACCINIUM VITIS-IDAEA LEAF (UNII: FO2ACM0RMQ)
- VACCINIUM VITIS-IDAEA LEAF (UNII: FO2ACM0RMQ) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- SENNA LEAF (UNII: AK7JF626KX)
- SENNA LEAF (UNII: AK7JF626KX) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
Which are S01 Allerdrain 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)
* 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".