NDC 60512-8035 Diamite
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60512 - Homeolab Usa Inc
- 60512-8035 - Diamite
Product Characteristics
Product Packages
NDC Code 60512-8035-5
Package Description: 125 TABLET, CHEWABLE in 1 JAR
NDC Code 60512-8035-6
Package Description: 500 TABLET, CHEWABLE in 1 JAR
Product Details
What is NDC 60512-8035?
What are the uses for Diamite?
Which are Diamite UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- CALCIUM PHOSPHATE (UNII: 97Z1WI3NDX)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CALCIUM SULFATE (UNII: WAT0DDB505)
- FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- POTASSIUM SULFATE (UNII: 1K573LC5TV)
- SULFATE ION (UNII: 7IS9N8KPMG) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC (UNII: A1Y870209Z)
- MAGNESIUM PHOSPHATE, DIBASIC (UNII: A1Y870209Z) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Diamite 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
* 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".