NDC 68093-7226 Mg217 Psoriasis Multi Symptom
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Product Details
What is NDC 68093-7226?
What are the uses for Mg217 Psoriasis Multi Symptom?
Which are Mg217 Psoriasis Multi Symptom UNII Codes?
The UNII codes for the active ingredients in this product are:
- COAL TAR (UNII: R533ESO2EC)
- COAL TAR (UNII: R533ESO2EC) (Active Moiety)
Which are Mg217 Psoriasis Multi Symptom 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)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- PROPANEDIOL (UNII: 5965N8W85T)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- EDETATE CALCIUM DISODIUM (UNII: 25IH6R4SGF)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Mg217 Psoriasis Multi Symptom?
- RxCUI: 1721271 - MG217 Psoriasis Coal Tar 2 % Topical Gel
- RxCUI: 1721271 - coal tar 0.02 MG/MG Topical Gel [MG217 Psoriasis Coal Tar]
- RxCUI: 1721271 - MG217 Psoriasis Coal Tar 0.02 MG/MG Topical Gel
- RxCUI: 245625 - coal tar 2 % Topical Gel
- RxCUI: 245625 - coal tar 0.02 MG/MG Topical Gel
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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".