NDC 68828-055 Calming Dynamics Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68828-055?
What are the uses for Calming Dynamics Spf 15?
Which are Calming Dynamics 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 Calming Dynamics 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)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- SQUALANE (UNII: GW89575KF9)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- TRIDECYL NEOPENTANOATE (UNII: 3Z8H1DA7J5)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- OAT (UNII: Z6J799EAJK)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- HEMIDESMUS INDICUS ROOT (UNII: Y5CFT48S90)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- PANTHENOL (UNII: WV9CM0O67Z)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
- PEG-4 LAURATE (UNII: AYF4VM3N1Z)
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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".