NDC 73278-101 Total Muscle Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73278 - Nemadji Management Llc
- 73278-101 - Total Muscle Relief
Product Packages
NDC Code 73278-101-13
Package Description: 90 mL in 1 BOTTLE
Product Details
What is NDC 73278-101?
What are the uses for Total Muscle Relief?
Which are Total Muscle Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR OIL (UNII: 75IZZ8Y727)
- CAMPHOR OIL (UNII: 75IZZ8Y727) (Active Moiety)
Which are Total Muscle Relief 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:
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HEMP (UNII: TD1MUT01Q7)
- WITCH HAZEL (UNII: 101I4J0U34)
- SAGE (UNII: 065C5D077J)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCONUT OIL (UNII: Q9L0O73W7L)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- ALMOND OIL (UNII: 66YXD4DKO9)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Total Muscle Relief?
- RxCUI: 1874891 - camphor 0.4 % / menthol 3.9 % Topical Gel
- RxCUI: 1874891 - camphor 0.004 MG/MG / menthol 0.039 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".