NDC 72519-105 Xceptol Pain Unscented
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72519 - Xceptor Llc
- 72519-105 - Xceptol Pain
Product Packages
NDC Code 72519-105-11
Package Description: 1 mL in 1 PACKET
NDC Code 72519-105-21
Package Description: 30 mL in 1 BOTTLE, DISPENSING
NDC Code 72519-105-22
Package Description: 50 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 72519-105?
What are the uses for Xceptol Pain Unscented?
Which are Xceptol Pain Unscented UNII Codes?
The UNII codes for the active ingredients in this product are:
- TROLAMINE SALICYLATE (UNII: H8O4040BHD)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Xceptol Pain Unscented 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)
- BETAINE (UNII: 3SCV180C9W)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- COCONUT OIL (UNII: Q9L0O73W7L)
- GAMMA CYCLODEXTRIN (UNII: KZJ0BYZ5VA)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISODODECANE (UNII: A8289P68Y2)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- QUATERNIUM-91 (UNII: 00J8H295NB)
- SHEA BUTTER ETHYL ESTERS (UNII: V2CI786FPG)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SORBIC ACID (UNII: X045WJ989B)
- TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".