NDC 63083-6005 Asbestox 6005
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-6005 - Asbestox
Product Packages
NDC Code 63083-6005-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-6005?
What are the uses for Asbestox 6005?
Which are Asbestox 6005 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- BEEF LUNG (UNII: 2I1RTO1MBR)
- BEEF LUNG (UNII: 2I1RTO1MBR) (Active Moiety)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- FERULA ASSA-FOETIDA RESIN (UNII: W9FZA51AS1)
- FERULA ASSA-FOETIDA RESIN (UNII: W9FZA51AS1) (Active Moiety)
- MOSCHUS MOSCHIFERUS MUSK SAC RESIN (UNII: 8KFK4W7KP7)
- MOSCHUS MOSCHIFERUS MUSK SAC RESIN (UNII: 8KFK4W7KP7) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- AMOSITE (UNII: 321T905Y7I)
- AMOSITE (UNII: 321T905Y7I) (Active Moiety)
Which are Asbestox 6005 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".