NDC 52261-5200 My Hemp Md
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 52261-5200?
What are the uses for My Hemp Md?
Which are My Hemp Md UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are My Hemp Md 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)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PANTHENOL (UNII: WV9CM0O67Z)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- SHEA BUTTER (UNII: K49155WL9Y)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- CASTOR OIL (UNII: D5340Y2I9G)
- TEA TREE OIL (UNII: VIF565UC2G)
- .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
- HEMP (UNII: TD1MUT01Q7)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- LAURETH-7 (UNII: Z95S6G8201)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
* 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".