NDC 69934-001 Xjow
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What is NDC 69934-001?
What are the uses for Xjow?
Which are Xjow UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Xjow 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:
- ELEUTHERO (UNII: ZQH6VH092Z)
- AMBER (UNII: 70J9Z0J26P)
- ANGELICA ROOT OIL (UNII: B25G881UOX)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- CHINESE CINNAMON LEAF OIL (UNII: 4U4V2F2E4Y)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- MYRRH (UNII: JC71GJ1F3L)
- CORYDALIS YANHUSUO TUBER (UNII: 0TUP42692Z)
- TURMERIC (UNII: 856YO1Z64F)
- DAEMONOROPS DRACO RESIN (UNII: 787Z7N9UCU)
- DIPSACUS FULLONUM ROOT (UNII: 4TJV827BQT)
- DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)
- ALCOHOL (UNII: 3K9958V90M)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- EUCOMMIA ULMOIDES LEAF (UNII: AM272O881C)
- GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)
- SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- ORCHIS MASCULA FLOWER (UNII: 6H1JQK35LA)
- PAEONIA OFFICINALIS ROOT (UNII: 8R564U2E1P)
- PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PRUNUS PERSICA SEED (UNII: V9C81470RR)
- RHEUM PALMATUM ROOT (UNII: G025DAL7CE)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Xjow?
- RxCUI: 866128 - menthol 1.25 % Topical Gel
- RxCUI: 866128 - menthol 0.0125 MG/MG Topical Gel
* 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".