NDC 57520-0522 Allersode II
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0522 - Allersode
Product Packages
NDC Code 57520-0522-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57520-0522?
What are the uses for Allersode II?
Which are Allersode II UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK)
- PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (Active Moiety)
- FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4)
- FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (Active Moiety)
- JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR)
- JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (Active Moiety)
- SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN)
- SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (Active Moiety)
- ACER NEGUNDO POLLEN (UNII: P6K070AR8V)
- ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (Active Moiety)
- POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP)
- POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (Active Moiety)
- BETULA OCCIDENTALIS POLLEN (UNII: R889N2L976)
- BETULA OCCIDENTALIS POLLEN (UNII: R889N2L976) (Active Moiety)
- QUERCUS RUBRA POLLEN (UNII: SVW19ET93C)
- QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (Active Moiety)
- CARYA OVATA POLLEN (UNII: 54UN9R2798)
- CARYA OVATA POLLEN (UNII: 54UN9R2798) (Active Moiety)
- POA PRATENSIS (UNII: 7EA48700V9)
- POA PRATENSIS (UNII: 7EA48700V9) (Active Moiety)
- DACTYLIS GLOMERATA (UNII: J41552QKAK)
- DACTYLIS GLOMERATA (UNII: J41552QKAK) (Active Moiety)
- AGROSTIS GIGANTEA (UNII: A5ODF78EPD)
- AGROSTIS GIGANTEA (UNII: A5ODF78EPD) (Active Moiety)
- PHLEUM PRATENSE (UNII: S7PW24BX20)
- PHLEUM PRATENSE (UNII: S7PW24BX20) (Active Moiety)
- AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y)
- AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (Active Moiety)
- AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX)
- AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (Active Moiety)
- AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L)
- AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
- RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW)
- RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (Active Moiety)
- RUMEX CRISPUS POLLEN (UNII: V825XJG64G)
- RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (Active Moiety)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (Active Moiety)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (Active Moiety)
Which are Allersode II 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)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".