NDC 62654-313 Dermacen Protectant
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 62654-313?
What are the uses for Dermacen Protectant?
Which are Dermacen Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Dermacen Protectant 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:
- QUADROSILAN (UNII: C5KT601WPM)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- MINERAL OIL (UNII: T5L8T28FGP)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CORN OIL (UNII: 8470G57WFM)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Dermacen Protectant?
- RxCUI: 1191136 - zinc oxide 5 % Rectal Cream
- RxCUI: 1191136 - zinc oxide 50 MG/ML Rectal Cream
- RxCUI: 1191136 - ZNO 50 MG/ML Rectal Cream
* 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".