NDC 73672-987 Pain Relief Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73672 - Hempfusion, Inc.
- 73672-987 - Pain Relief Cream
Product Packages
NDC Code 73672-987-50
Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE
Product Details
What is NDC 73672-987?
What are the uses for Pain Relief Cream?
Which are Pain Relief Cream 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 Cream 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:
- COCO-CAPRYLATE (UNII: 4828G836N6)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- HEMP (UNII: TD1MUT01Q7)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- BLACK PEPPER OIL (UNII: U17J84S19Z)
- MYELOPEROXIDASE (UNII: JQZ6YM58U5)
- GLUCOSE OXIDASE (UNII: 0T8392U5N1)
- DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO)
- WATER (UNII: 059QF0KO0R)
- PEPPERMINT (UNII: V95R5KMY2B)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- ALOE (UNII: V5VD430YW9)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CLOVE OIL (UNII: 578389D6D0)
- 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".