NDC 62742-4177 Cannaflex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 62742-4177?
What are the uses for Cannaflex?
Which are Cannaflex 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 Cannaflex 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERIN (UNII: PDC6A3C0OX)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- ROSA MOSCHATA SEED OIL (UNII: T031ZE559T)
- 3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- MENTHOL (UNII: L7T10EIP3A)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)
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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".