NDC 42248-123 Drymarine Age Control
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42248 - Zenith Medicosm Sl
- 42248-123 - Drymarine
Product Packages
NDC Code 42248-123-01
Package Description: 200 mL in 1 TUBE
Product Details
What is NDC 42248-123?
Which are Drymarine Age Control UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Drymarine Age Control 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:
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRICAPRYLIN (UNII: 6P92858988)
- WATER (UNII: 059QF0KO0R)
- SQUALANE (UNII: GW89575KF9)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PEG-8 STEARATE (UNII: 2P9L47VI5E)
- TROLAMINE (UNII: 9O3K93S3TK)
- GLYCERIN (UNII: PDC6A3C0OX)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- HYDROLYZED ELASTIN, BOVINE, ALKALINE (1000 MW) (UNII: ZR28QKN0WT)
- CARBOMER 934 (UNII: Z135WT9208)
- SHEA BUTTER (UNII: K49155WL9Y)
- PEG/PPG-20/6 DIMETHICONE (UNII: PWZ7N4UIKE)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W)
- PEG-32 STEARATE (UNII: 33GX5WQC0M)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- OAT (UNII: Z6J799EAJK)
- ROYAL JELLY (UNII: L497I37F0C)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- ALLANTOIN (UNII: 344S277G0Z)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- LEVOMENOL (UNII: 24WE03BX2T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LIMONENE, (+/-)- (UNII: 9MC3I34447)
- BENZYL BENZOATE (UNII: N863NB338G)
- GERANIOL (UNII: L837108USY)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- EUGENOL (UNII: 3T8H1794QW)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- CITRAL (UNII: T7EU0O9VPP)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
* 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".