NDC 72519-104 Xceptor Cbd Pain Menthol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72519 - Xceptor Llc
- 72519-104 - Xceptor Cbd Pain
Product Packages
NDC Code 72519-104-21
Package Description: 30 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 72519-104?
What are the uses for Xceptor Cbd Pain Menthol?
Which are Xceptor Cbd Pain Menthol 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 Cbd Pain Menthol 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BETA VULGARIS (UNII: 4G174V5051)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- COCONUT OIL (UNII: Q9L0O73W7L)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- BETADEX (UNII: JV039JZZ3A)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- SHEA BUTTER (UNII: K49155WL9Y)
- SORBIC ACID (UNII: X045WJ989B)
- TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)
- XANTHAN GUM (UNII: TTV12P4NEE)
- WATER (UNII: 059QF0KO0R)
* 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".