NDC 68678-039 Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68678 - Ahc Ventures Corp Dba Cry
- 68678-039 - Pain Relieving
Product Characteristics
Product Packages
NDC Code 68678-039-04
Package Description: 112 mL in 1 BOTTLE, DISPENSING
NDC Code 68678-039-16
Package Description: 449 mL in 1 BOTTLE, DISPENSING
NDC Code 68678-039-99
Package Description: 3.35 mL in 1 PACKET
Product Details
What is NDC 68678-039?
What are the uses for Pain Relieving?
Which are Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Pain Relieving 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA (UNII: O80TY208ZW)
- BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CITRUS AURANTIUM FRUIT (UNII: DQD16J2B5O)
- GRAPEFRUIT (UNII: O82C39RR8C)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- TROLAMINE (UNII: 9O3K93S3TK)
- YUCCA SCHIDIGERA (UNII: 08A0YG3VIC)
* 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".