NDC 44911-0547 Weed Grass Antigens
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44911 - Energique, Inc.
- 44911-0547 - Weed Grass Antigens
Product Packages
NDC Code 44911-0547-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 44911-0547?
What are the uses for Weed Grass Antigens?
Which are Weed Grass Antigens UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI)
- PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (Active Moiety)
- ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0)
- ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0) (Active Moiety)
- WORMWOOD (UNII: F84709P2XV)
- WORMWOOD (UNII: F84709P2XV) (Active Moiety)
- AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
- AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
- MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)
- ALFALFA (UNII: DJO934BRBD) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC) (Active Moiety)
- BAMBUSA BAMBOS STEM (UNII: NRA4497HC5)
- BAMBUSA BAMBOS STEM (UNII: NRA4497HC5) (Active Moiety)
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89)
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89) (Active Moiety)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
- DACTYLIS GLOMERATA TOP (UNII: J41552QKAK)
- DACTYLIS GLOMERATA TOP (UNII: J41552QKAK) (Active Moiety)
- CYNODON DACTYLON POLLEN (UNII: 175F461W10)
- CYNODON DACTYLON WHOLE (UNII: 2Q8MR21NHK) (Active Moiety)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
- SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O)
- SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O) (Active Moiety)
- ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y)
- ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y) (Active Moiety)
- PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK)
- PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (Active Moiety)
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
- PHLEUM PRATENSE TOP (UNII: S7PW24BX20) (Active Moiety)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK)
- SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
- TRIFOLIUM REPENS FLOWER (UNII: 49Y788T742)
- TRIFOLIUM REPENS FLOWER (UNII: 49Y788T742) (Active Moiety)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (Active Moiety)
Which are Weed Grass Antigens 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".