NDC 78232-002 Muscle And Joint Pain Relief Gr Isolate 750 Mg
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78232 - Clarity Labs Llc
- 78232-002 - Muscle And Joint Pain Relief Gr Isolate 750 Mg
Product Packages
NDC Code 78232-002-03
Package Description: 120 BOX in 1 CARTON / 30 TUBE in 1 BOX (78232-002-02) / 30 g in 1 TUBE (78232-002-01)
Product Details
What is NDC 78232-002?
What are the uses for Muscle And Joint Pain Relief Gr Isolate 750 Mg?
Which are Muscle And Joint Pain Relief Gr Isolate 750 Mg UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Muscle And Joint Pain Relief Gr Isolate 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:
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- CUCUMBER (UNII: YY7C30VXJT)
- WATER (UNII: 059QF0KO0R)
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- BENTONITE (UNII: A3N5ZCN45C)
- CHAMOMILE (UNII: FGL3685T2X)
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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".