NDC 52261-5202 My Hemp Md Cbd Muscle And Deep Tissue Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52261 - Cosco International, Inc.
- 52261-5202 - My Hemp Md Cbd Muscle And Deep Tissue Cream
Product Packages
NDC Code 52261-5202-1
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON / .075 kg in 1 BOTTLE, WITH APPLICATOR (52261-5202-0)
Product Details
What is NDC 52261-5202?
What are the uses for My Hemp Md Cbd Muscle And Deep Tissue Cream?
Which are My Hemp Md Cbd Muscle And Deep Tissue Cream 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 My Hemp Md Cbd Muscle And Deep Tissue 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:
- WATER (UNII: 059QF0KO0R)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- HEMP (UNII: TD1MUT01Q7)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
- CAMPHOR OIL (UNII: 75IZZ8Y727)
- CLOVE LEAF OIL (UNII: VCA5491KVF)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
* Please review the disclaimer below.
[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".