NDC 69701-8623 Neuro Max Pain And Muscle Relief Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69701 - Starman Consulting Llc
- 69701-8623 - Neuro Max Pain And Muscle Relief Gel
Product Packages
NDC Code 69701-8623-5
Package Description: 85 g in 1 TUBE
Product Details
What is NDC 69701-8623?
What are the uses for Neuro Max Pain And Muscle Relief Gel?
Which are Neuro Max Pain And Muscle Relief Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Neuro Max Pain And Muscle 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:
- ALCOHOL (UNII: 3K9958V90M)
- ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
- APHANIZOMENON FLOS-AQUAE (UNII: 49VG1X560X)
- AVENA SATIVA LEAF (UNII: 206PI19V7R)
- CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- SILYBUM MARIANUM LEAF (UNII: K93P558418)
- STELLARIA MEDIA LEAF (UNII: E6M924345X)
- ULMUS RUBRA BARK (UNII: 91QY4PXU8Q)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- DISODIUM HEDTA (UNII: KME849MC7A)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL DILAURATE (UNII: MFL3ZIE8SK)
- GLYCERYL LAURATE (UNII: Y98611C087)
- HYDROXYPROPYL CELLULOSE (TYPE M) (UNII: U3JF91U133)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- WATER (UNII: 059QF0KO0R)
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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".