NDC 51393-6543 Eczema Cleanse
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 51393-6543?
What are the uses for Eczema Cleanse?
Which are Eczema Cleanse UNII Codes?
The UNII codes for the active ingredients in this product are:
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC)
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (Active Moiety)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
Which are Eczema Cleanse 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:
- SODIUM PALMATE (UNII: S0A6004K3Z)
- SODIUM COCOATE (UNII: R1TQH25F4I)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SESAME OIL (UNII: QX10HYY4QV)
- LAVANDIN OIL (UNII: 9RES347CKG)
- PALMAROSA OIL (UNII: 0J3G3O53ST)
- WHITE PINE OIL (UNII: HA5CX6676U)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- NIAOULI OIL (UNII: D50IC2T8FU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- URTICA DIOICA (UNII: 710FLW4U46)
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[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".