NDC 68828-163 Harmony Dynamics Facial Boosting Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68828-163?
What are the uses for Harmony Dynamics Facial Boosting Spf 15?
Which are Harmony Dynamics Facial Boosting Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Harmony Dynamics Facial Boosting Spf 15 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)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARYL STEARATE (UNII: 5WX2EGD0DK)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- GARCINIA INDICA SEED BUTTER (UNII: US2H3D7800)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIMETHICONOL (250000 MW) (UNII: RKI3S914RT)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- DIGLYCERIN (UNII: 3YC120743U)
- SHEA BUTTER (UNII: K49155WL9Y)
- SPANISH CHESTNUT (UNII: 2MT5XMR2YW)
- LICORICE (UNII: 61ZBX54883)
- MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B)
- VETIVERIA ZIZANIOIDES ROOT (UNII: 37TB8LUP9Z)
- WITHANIA SOMNIFERA LEAF (UNII: J337CNM3CW)
- PEPPERMINT (UNII: V95R5KMY2B)
- CERAMIDE 2 (UNII: C04977SRJ5)
- CAMPESTEROL (UNII: 5L5O665639)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SOYBEAN (UNII: L7HT8F1ZOD)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ALCOHOL (UNII: 3K9958V90M)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- PANTHENOL (UNII: WV9CM0O67Z)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- PEG-4 LAURATE (UNII: AYF4VM3N1Z)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- EDETATE TRISODIUM (UNII: 420IP921MB)
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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".