PRESTIGE CAVIAR SUPER AQUA SERUM- niacinamide, adenosine cream

Prestige Caviar Super Aqua Serum by

Drug Labeling and Warnings

Prestige Caviar Super Aqua Serum by is a Otc medication manufactured, distributed, or labeled by FW1 R&D_Branch, Cosmax, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Niacinamide 2.00%
Adenosine 0.04%

PURPOSE

Skin Protectant

INDICATIONS & USAGE

To provide hydration and promote attractiveness to skin

DOSAGE & ADMINISTRATION

Apply gently over clean, dry skin or/and desired area 1 to 2 times daily

For morning and evening use

WARNINGS

For external use only.
Do not use on damaged or broken skin.
When using this product, keep out of eyes. Rinse with water to remove
Stop using and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Caviar Extract, Butylene Glycol, Water, Glycerin, Glycereth-26, Linum Usitatissimum (Linseed) Seed Extract, 1,2-Hexanediol, Pentylene Glycol, Polyglycerin-3, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate, Phenoxyethanol, PEG-60 Hydrogenated Castor Oil, Carbomer, Tromethamine
, Panthenol, Diphenyl Dimethicone, Triethylhexanoin, Fragrance(Parfum), Acacia Senegal Gum, Polyglutamic Acid, Hydrogenated Lecithin, Disodium EDTA, Peat Water, Citric Acid, Hydroxypropyl Methylcellulose, Rosmarinus Officinalis (Rosemary) Leaf Oil, Polydecene, Saccharide Isomerate, Potassium Sorbate, Hydrolyzed Myrtus Communis Leaf Extract, Caprylic/Capric Triglyceride, Zingiber Officinale (Ginger) Root Extract, Sorbitan Laurate, Squalane, Viscum Album (Mistletoe) Fruit Extract, Pancratium Maritimum Extract, Ethylhexylglycerin, Ceramide 3, Hydroxyethylcellulose, Acetyl Dipeptide-1 Cetyl Ester, Sodium Citrate, Prunus Persica (Peach) Flower Extract

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PRESTIGE CAVIAR SUPER AQUA SERUM 
niacinamide, adenosine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70519-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	1 mg  in 50 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.02 mg  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70519-005-02	1 in 1 PACKAGE	06/27/2017
1	NDC: 70519-005-01	50 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/27/2017

Labeler - FW1 R&D_Branch (689605458)

Registrant - FW1 R&D_Branch (689605458)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmax, Inc		689049693	manufacture(70519-005)