NDC 81799-010 Nupharmisto Psoriasis Eczema Cream
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What is NDC 81799-010?
What are the uses for Nupharmisto Psoriasis Eczema Cream?
Which are Nupharmisto Psoriasis Eczema Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHA CANADENSIS TOP (UNII: 610T51U707)
- MENTHA CANADENSIS TOP (UNII: 610T51U707) (Active Moiety)
- VIOLA PHILIPPICA WHOLE (UNII: O176VC3N54)
- VIOLA PHILIPPICA WHOLE (UNII: O176VC3N54) (Active Moiety)
- SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)
- SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L) (Active Moiety)
- RHINACANTHUS NASUTUS LEAF (UNII: 97OQD55S9I)
- RHINACANTHUS NASUTUS LEAF (UNII: 97OQD55S9I) (Active Moiety)
- DICTAMNUS DASYCARPUS WHOLE (UNII: IM7ZCU30YH)
- DICTAMNUS DASYCARPUS WHOLE (UNII: IM7ZCU30YH) (Active Moiety)
- EUPHORBIA HIRTA (UNII: L13YF113GN)
- EUPHORBIA HIRTA (UNII: L13YF113GN) (Active Moiety)
- MURRAYA PANICULATA FRUIT (UNII: PE014Z7R7C)
- MURRAYA PANICULATA FRUIT (UNII: PE014Z7R7C) (Active Moiety)
Which are Nupharmisto Psoriasis Eczema Cream 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:
- BORNEOL (UNII: M89NIB437X)
- SMILAX GLABRA WHOLE (UNII: H51N91QNEB)
- CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)
- SCOPARIA DULCIS LEAF (UNII: 1PD9Z8123P)
- SOLIDAGO DECURRENS WHOLE (UNII: Y026RJV99T)
- WATER (UNII: 059QF0KO0R)
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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".