NDC 72800-003 Joint And Muscle Relief 750 Mg
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72800 - Lifecure Rx Specialty Pharmacy
- 72800-003 - Joint And Muscle Relief 750 Mg
Product Packages
NDC Code 72800-003-50
Package Description: 50 mL in 1 BOTTLE
Product Details
What is NDC 72800-003?
What are the uses for Joint And Muscle Relief 750 Mg?
Which are Joint And Muscle Relief 750 Mg UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Joint And Muscle Relief 750 Mg 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:
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- CARBOMER 934 (UNII: Z135WT9208)
- JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)
- HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
- ALCOHOL (UNII: 3K9958V90M)
- GERANIUM THUNBERGII FLOWERING TOP (UNII: 9IXM1668B6)
- HEMP (UNII: TD1MUT01Q7)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- OLEIC ACID (UNII: 2UMI9U37CP)
- 1,2-DILINOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE (UNII: 7L874P1M1O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Joint And Muscle Relief 750 Mg?
- RxCUI: 2119805 - lidocaine 2 % / menthol 3 % Topical Gel
- RxCUI: 2119805 - lidocaine 0.02 MG/MG / menthol 0.03 MG/MG Topical Gel
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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".