NDC 63083-6018 Tap Water Detox 6018
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 63083-6018?
What are the uses for Tap Water Detox 6018?
Which are Tap Water Detox 6018 UNII Codes?
The UNII codes for the active ingredients in this product are:
- 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN (UNII: DO80M48B6O)
- 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN (UNII: DO80M48B6O) (Active Moiety)
- BROMINE (UNII: SBV4XY874G)
- BROMINE (UNII: SBV4XY874G) (Active Moiety)
- CHLORINE (UNII: 4R7X1O2820)
- CHLORINE (UNII: 4R7X1O2820) (Active Moiety)
- CHLOROFORM (UNII: 7V31YC746X)
- CHLOROFORM (UNII: 7V31YC746X) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- FLUORIDE ION (UNII: Q80VPU408O)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- LEAD (UNII: 2P299V784P)
- LEAD (UNII: 2P299V784P) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) (Active Moiety)
- FENSON (UNII: DFC2HB4I0K)
- FENSON (UNII: DFC2HB4I0K) (Active Moiety)
Which are Tap Water Detox 6018 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:
- ALCOHOL (UNII: 3K9958V90M)
- 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".