NDC 72186-011 Retreat
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72186 - Key Origins, Inc.
- 72186-011 - Retreat
Product Packages
NDC Code 72186-011-11
Package Description: 30 mL in 1 JAR
Product Details
What is NDC 72186-011?
What are the uses for Retreat?
Which are Retreat 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, UNSPECIFIED FORM (UNII: 97Z1WI3NDX)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CALCIUM SULFATE, UNSPECIFIED FORM (UNII: WAT0DDB505)
- FERROUS PHOSPHATE (UNII: D07L04MRWI)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
- MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE (UNII: 453COF7817)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- HYDRATED SILICA (UNII: Y6O7T4G8P9) (Active Moiety)
- CENTAUREA BENEDICTA (UNII: 6L5ZL09795)
- CENTAUREA BENEDICTA (UNII: 6L5ZL09795) (Active Moiety)
Which are Retreat 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPANEDIOL (UNII: 5965N8W85T)
* 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".