NDC 81654-001 Moxa Roll
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 81654-001-01
Package Description: 600 BOTTLE in 1 BOX / 20 mL in 1 BOTTLE
Product Details
What is NDC 81654-001?
What are the uses for Moxa Roll?
Which are Moxa Roll UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARYOPHYLLENE (UNII: BHW853AU9H)
- CARYOPHYLLENE (UNII: BHW853AU9H) (Active Moiety)
- 4-TERPINEOL, (+/-)- (UNII: L65MV77ZG6)
- 4-TERPINEOL, (+/-)- (UNII: L65MV77ZG6) (Active Moiety)
Which are Moxa Roll 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:
- .ALPHA.-PHELLANDRENE (UNII: 49JV13XE39)
- .ALPHA.-CUBEBENE, (-)- (UNII: 438H9S5RG9)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- BORNEOL, (+)- (UNII: 8D24LWT4FK)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
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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".