NDC 73318-4321 Slmd Dual Defender Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 73318-4321?
What are the uses for Slmd Dual Defender Spf 30?
Which are Slmd Dual Defender Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Slmd Dual Defender Spf 30 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRIMETHOXYBENZYLIDENE PENTANEDIONE (UNII: 322V0ACF25)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- ALLANTOIN (UNII: 344S277G0Z)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PANTHENOL (UNII: WV9CM0O67Z)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PUMMELO (UNII: ET1TN5W71X)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- 1,3-BETA-GLUCAN SYNTHASE COMPONENT FKS1 (UNII: 4FRY3LJG0V)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
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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".