NDC 57520-0218 Allergy Composition
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0218 - Allergy Composition
Product Packages
NDC Code 57520-0218-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57520-0218?
What are the uses for Allergy Composition?
Which are Allergy Composition UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- TAURINE (UNII: 1EQV5MLY3D)
- TAURINE (UNII: 1EQV5MLY3D) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
- LEVODOPA (UNII: 46627O600J)
- LEVODOPA (UNII: 46627O600J) (Active Moiety)
- CHONDRUS (UNII: XR12Z4HLEA)
- CHONDRUS (UNII: XR12Z4HLEA) (Active Moiety)
Which are Allergy Composition 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".