NDC 69031-004 Soothion Psoriasis And Seborrheic Dermatitis Formula
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69031 - Electrolyzed Innovations, Llc
- 69031-004 - Soothion Psoriasis And Seborrheic Dermatitis Formula
Product Packages
NDC Code 69031-004-08
Package Description: 226 g in 1 BOTTLE
Product Details
What is NDC 69031-004?
What are the uses for Soothion Psoriasis And Seborrheic Dermatitis Formula?
Which are Soothion Psoriasis And Seborrheic Dermatitis Formula 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 Soothion Psoriasis And Seborrheic Dermatitis Formula 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:
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- IMIDUREA (UNII: M629807ATL)
- SHEANUT OIL (UNII: O88E196QRF)
- SPEARMINT OIL (UNII: C3M81465G5)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Soothion Psoriasis And Seborrheic Dermatitis Formula?
- RxCUI: 103568 - salicylic acid 2 % Topical Lotion
- RxCUI: 103568 - salicylic acid 20 MG/ML Topical Lotion
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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".