NDC 73615-103 Md Science Cannabidiol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73615 - Md Natural Health Llc
- 73615-103 - Md Science Cannabidiol
Product Characteristics
Product Packages
NDC Code 73615-103-03
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 88 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 73615-103?
What are the uses for Md Science Cannabidiol?
Which are Md Science Cannabidiol UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
Which are Md Science Cannabidiol 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- COCONUT OIL (UNII: Q9L0O73W7L)
- EMU OIL (UNII: 344821WD61)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SORBITOL (UNII: 506T60A25R)
- STEARETH-21 (UNII: 53J3F32P58)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
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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".