NDC 72617-4003 Allergy Mix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72617 - Asn
- 72617-4003 - Allergy Mix
Product Packages
NDC Code 72617-4003-3
Package Description: 1 BOTTLE in 1 PACKAGE / 15 mL in 1 BOTTLE
Product Details
What is NDC 72617-4003?
What are the uses for Allergy Mix?
Which are Allergy Mix UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (Active Moiety)
- PASSALORA FULVA (UNII: HR6H5057CO)
- PASSALORA FULVA (UNII: HR6H5057CO) (Active Moiety)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (Active Moiety)
- WHITE MULBERRY (UNII: MN25R0HH5A)
- WHITE MULBERRY (UNII: MN25R0HH5A) (Active Moiety)
- JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y)
- JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (Active Moiety)
- NERIUM OLEANDER FLOWER (UNII: WO4WVF1WVM)
- NERIUM OLEANDER FLOWER (UNII: WO4WVF1WVM) (Active Moiety)
- JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY)
- JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY) (Active Moiety)
- USTILAGO MAYDIS (UNII: 4K7Z7K7SWG)
- USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
Which are Allergy 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:
- WATER (UNII: 059QF0KO0R)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- SEA SALT (UNII: 87GE52P74G)
- POTASSIUM PHOSPHATE, MONOBASIC (UNII: 4J9FJ0HL51)
- SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)
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[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".