NDC 57955-6001 Indoor Air Pollution Detox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-6001 - Indoor Air Pollution Detox
Product Packages
NDC Code 57955-6001-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-6001?
What are the uses for Indoor Air Pollution Detox?
Which are Indoor Air Pollution Detox UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETALDEHYDE (UNII: GO1N1ZPR3B)
- ACETALDEHYDE (UNII: GO1N1ZPR3B) (Active Moiety)
- AMMONIA (UNII: 5138Q19F1X)
- AMMONIA (UNII: 5138Q19F1X) (Active Moiety)
- CARBON MONOXIDE (UNII: 7U1EE4V452)
- CARBON MONOXIDE (UNII: 7U1EE4V452) (Active Moiety)
- CHLOROFORM (UNII: 7V31YC746X)
- CHLOROFORM (UNII: 7V31YC746X) (Active Moiety)
- FORMALDEHYDE (UNII: 1HG84L3525)
- FORMALDEHYDE (UNII: 1HG84L3525) (Active Moiety)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- KEROSENE (UNII: 1C89KKC04E)
- KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
- LEAD (UNII: 2P299V784P)
- LEAD (UNII: 2P299V784P) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
Which are Indoor Air Pollution Detox 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)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
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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".