NDC 70519-005 Prestige Caviar Super Aqua Serum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70519 - Fw1 R&d_branch
- 70519-005 - Prestige Caviar Super Aqua Serum
Product Packages
NDC Code 70519-005-02
Package Description: 1 CONTAINER in 1 PACKAGE / 50 mL in 1 CONTAINER (70519-005-01)
Product Details
What is NDC 70519-005?
What are the uses for Prestige Caviar Super Aqua Serum?
Which are Prestige Caviar Super Aqua Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Prestige Caviar Super Aqua Serum 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:
- CAVIAR, UNSPECIFIED (UNII: 020K6HLU0O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERETH-26 (UNII: NNE56F2N14)
- FLAX SEED (UNII: 4110YT348C)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- TROMETHAMINE (UNII: 023C2WHX2V)
- PANTHENOL (UNII: WV9CM0O67Z)
- DIPHENYL DIMETHICONE (400 CST) (UNII: Y5MXX82OQ7)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- ACACIA (UNII: 5C5403N26O)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- HYDROGENATED DIDECENE (UNII: 048B98MT5O)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- MYRTUS COMMUNIS LEAF (UNII: U20N87188F)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GINGER (UNII: C5529G5JPQ)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- SQUALANE (UNII: GW89575KF9)
- VISCUM ALBUM FRUIT (UNII: P83EQ521R3)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CERAMIDE NP (UNII: 4370DF050B)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- ACETYL TYROSYLARGININE CETYL ESTER (UNII: 3M7W78X5IR)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- PRUNUS PERSICA FLOWER (UNII: 19GWB0JENH)
* 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".