NDC 57955-3400 Aller Detox Water Chemicals
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-3400 - Aller Detox Water Chemicals
Product Packages
NDC Code 57955-3400-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-3400?
What are the uses for Aller Detox Water Chemicals?
Which are Aller Detox Water Chemicals UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
- KAOLIN (UNII: 24H4NWX5CO)
- KAOLIN (UNII: 24H4NWX5CO) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- BROMINE (UNII: SBV4XY874G)
- BROMINE (UNII: SBV4XY874G) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CHIMAPHILA UMBELLATA (UNII: WCK21A9W9J)
- CHIMAPHILA UMBELLATA (UNII: WCK21A9W9J) (Active Moiety)
- CHLORINE (UNII: 4R7X1O2820)
- CHLORINE (UNII: 4R7X1O2820) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- LEMNA MINOR (UNII: 621HHM46SV)
- LEMNA MINOR (UNII: 621HHM46SV) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- LEAD (UNII: 2P299V784P)
- LEAD (UNII: 2P299V784P) (Active Moiety)
- STRYCHNINE (UNII: H9Y79VD43J)
- STRYCHNINE (UNII: H9Y79VD43J) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
Which are Aller Detox Water Chemicals 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)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".