NDC 73672-989 Pain Relief Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 73672-989?
What are the uses for Pain Relief Gel?
Which are Pain Relief Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Pain Relief Gel 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:
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- HEMP (UNII: TD1MUT01Q7)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- ALOE (UNII: V5VD430YW9)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- CLOVE OIL (UNII: 578389D6D0)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- WATER (UNII: 059QF0KO0R)
- CAPSICUM (UNII: 00UK7646FG)
- GINGER (UNII: C5529G5JPQ)
- TURMERIC OIL (UNII: 6KGS8SP16U)
- MYELOPEROXIDASE (UNII: JQZ6YM58U5)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BLACK PEPPER OIL (UNII: U17J84S19Z)
- BETASIZOFIRAN (UNII: 2X51AD1X3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- PULLULAN (UNII: 8ZQ0AYU1TT)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GLUCOSE OXIDASE (UNII: 0T8392U5N1)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- LYSOPHOSPHATIDYLCHOLINE, SOYBEAN (UNII: CQD833204Z)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
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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".