NDC 57955-6497 Dust Mite And Roach Allergy Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-6497 - Dust Mite And Roach Allergy Relief
Product Packages
NDC Code 57955-6497-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-6497?
What are the uses for Dust Mite And Roach Allergy Relief?
Which are Dust Mite And Roach Allergy Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (Active Moiety)
- PERIPLANETA AMERICANA (UNII: 2RQ1L9N089)
- PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (Active Moiety)
- BLATTA ORIENTALIS (UNII: 535787266D)
- BLATTA ORIENTALIS (UNII: 535787266D) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- FLAX SEED (UNII: 4110YT348C)
- FLAX SEED (UNII: 4110YT348C) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
Which are Dust Mite And Roach Allergy Relief 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
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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".