NDC 63302-202 Dermazor Psoriasis And Seborrheic Dermatitis
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What is NDC 63302-202?
What are the uses for Dermazor Psoriasis And Seborrheic Dermatitis?
Which are Dermazor Psoriasis And Seborrheic Dermatitis UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Dermazor Psoriasis And Seborrheic Dermatitis 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:
- LANOLIN (UNII: 7EV65EAW6H)
- PETROLATUM (UNII: 4T6H12BN9U)
- WATER (UNII: 059QF0KO0R)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- STARCH, CORN (UNII: O8232NY3SJ)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- WHITE WAX (UNII: 7G1J5DA97F)
- POLYSORBATE 65 (UNII: 14BGY2Y3MJ)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SILYBUM MARIANUM SEED OIL (UNII: NYY23HEN06)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- VITAMIN A (UNII: 81G40H8B0T)
- VITAMIN D (UNII: 9VU1KI44GP)
- BORAGE SEED OIL (UNII: F8XAG1755S)
- ALMOND OIL (UNII: 66YXD4DKO9)
- LEVOMENOL (UNII: 24WE03BX2T)
- NIGELLA SATIVA SEED OIL (UNII: CS4U38E731)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
What is the NDC to RxNorm Crosswalk for Dermazor Psoriasis And Seborrheic Dermatitis?
- RxCUI: 1537091 - Dermazor 3 % Topical Cream
- RxCUI: 1537091 - salicylic acid 30 MG/ML Topical Cream [Dermazor]
- RxCUI: 1537091 - Dermazor 30 MG/ML Topical Cream
- RxCUI: 416910 - salicylic acid 3 % Topical Cream
- RxCUI: 416910 - salicylic acid 30 MG/ML Topical Cream
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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".