NDC 72519-101 Xceptor Pain
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 72519-101?
What are the uses for Xceptor Pain?
Which are Xceptor Pain UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Xceptor Pain 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)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GAMMA CYCLODEXTRIN (UNII: KZJ0BYZ5VA)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- BETAINE (UNII: 3SCV180C9W)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- COCONUT OIL (UNII: Q9L0O73W7L)
- HYALURONIC ACID (UNII: S270N0TRQY)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- OLEIC ACID (UNII: 2UMI9U37CP)
- PALMITIC ACID (UNII: 2V16EO95H1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CANOLA OIL (UNII: 331KBJ17RK)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBIC ACID (UNII: X045WJ989B)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Xceptor Pain?
- RxCUI: 311635 - methyl salicylate 10 % Topical Cream
- RxCUI: 311635 - methyl salicylate 100 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".