NDC 53208-545 Soorhyehan Onbit Two Way Cake 23
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Product Details
What is NDC 53208-545?
Which are Soorhyehan Onbit Two Way Cake 23 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Soorhyehan Onbit Two Way Cake 23 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:
- TALC (UNII: 7SEV7J4R1U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- MICA (UNII: V8A1AW0880)
- TRICHOSANTHES KIRILOWII ROOT (UNII: V409XGE0TS)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CAROB (UNII: 5MG5Z946UO)
- PALMITIC ACID (UNII: 2V16EO95H1)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- HONEY (UNII: Y9H1V576FH)
- BAMBUSA VULGARIS SAP (UNII: 26W4035XBO)
- PATCHOULI OIL (UNII: F3IN55X5PO)
- PRUNUS ARMENIACA SEED (UNII: 75356789IW)
- LIGUSTICUM TENUISSIMUM ROOT (UNII: 2O0H84E074)
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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".