NDC 43251-2231 Flexitol Naturals Eczema And Psoriasis
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43251 - Lacorium Health International Pty Ltd
- 43251-2231 - Flexitol Naturals Eczema And Psoriasis
Product Packages
NDC Code 43251-2231-1
Package Description: 1 TUBE in 1 CARTON / 56 g in 1 TUBE
NDC Code 43251-2231-2
Package Description: 1 g in 1 PACKET
Product Details
What is NDC 43251-2231?
What are the uses for Flexitol Naturals Eczema And Psoriasis?
Which are Flexitol Naturals Eczema And Psoriasis UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- POTASSIUM SULFATE (UNII: 1K573LC5TV)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
Which are Flexitol Naturals Eczema And Psoriasis 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:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- COCOA BUTTER (UNII: 512OYT1CRR)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- SHEA BUTTER (UNII: K49155WL9Y)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- 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".