NDC 73072-001 Mans Best Friend
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 73072-001?
What are the uses for Mans Best Friend?
Which are Mans Best Friend UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Mans Best Friend 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)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
- LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- ALLANTOIN (UNII: 344S277G0Z)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BIOSACCHARIDE GUM-4 (UNII: 9XRL057X90)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- MORINGA OLEIFERA SEED OIL (UNII: REM6A5QMC0)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
* 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".