NDC 68647-167 Hayfever Fighter
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Product Details
What is NDC 68647-167?
What are the uses for Hayfever Fighter?
Which are Hayfever Fighter UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- AMERICAN ELDERBERRY (UNII: 7610Y219OC)
- AMERICAN ELDERBERRY (UNII: 7610Y219OC) (Active Moiety)
Which are Hayfever Fighter 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:
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- WATER (UNII: 059QF0KO0R)
* 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".