P1P SKIN REBIRTH CREAM- dimethicone, adenosine cream

P1P Skin Rebirth Cream by

Drug Labeling and Warnings

P1P Skin Rebirth Cream by is a Otc medication manufactured, distributed, or labeled by Phytos Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

P1P Skin Rebirth Cream

Dimethicone (1%)Adenosine (0.4%) 

skin protectant

Keep out of reach of children- Do not swallow. In case of accidental ingestion, seek professional assistance.

Moisturizes Skin

WarningsFor external use onlyDo not use when Your skin is red, inflamed, irritated or painfulWhen using this product- Do not apply on other parts of the body- Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.- Do not apply directly to wound or open cut.Stop use and ask doctor if rash or irritation on skin develops and lasts.Store at room temperature 

Apply moderate amount gently on face

Water, Glycerin, Caprylic/Capric Triglyceride, Butylene Glycol, Tremella Fuciformis (Mushroom) Extract, Glyceryl Polyacrylate, Sodium Hyaluronate (1%), Centella Asiatica Extract, Limnanthes Alba (Meadowfoam) Seed Oil, Palmitoyl Oligopeptide, Palmitoyl Tetrapeptide-7, Cetyl Ethylhexanoate, Lactoglobulin, Sodium Dehydroacetate, Cetearyl Alcohol, Glyceryl Stearate, Phytosteryl/Decyltetradecyl Myristoyl Methyl Beta-Alaninate, Stearic Acid, Tocopheryl Acetate, Totarol, Batyl Alcohol, Lecithin, Arginine, Ethyl Ascorbyl Ether, Carbomer, Phytosphingosine Phosphate, Poloxamer 407, Polysorbate80, 1,2-Hexanediol, Isododecane, Vinyl Dimethicone/Lauryl DimethiconeCrosspolymer, Lauryl Dimethicone, Citrus Paradisi (Grapefruit)Seed Extract, Artemisia Vulgaris Extract, Octanediol, Ethylhexylglycerin, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Polysorbate20, Sodium Ascorbyl Phosphate, Bacillus/Soybean/Folic Acid Ferment Extract, Acetyl Glutamine, rh-Oligopeptide-1, rh-Oligopeptide-2, rh-Polypeptide-1, rh-Polypeptide-11, rh-Polypeptide-9, Disodium EDTA

INGREDIENTS AND APPEARANCE

P1P SKIN REBIRTH CREAM 
dimethicone, adenosine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69579-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	dimethicone	0.01   in 30 mL
adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	adenosine	0.004   in 30 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
glycerin (UNII: PDC6A3C0OX)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
cetyl ethylhexanoate (UNII: 134647WMX4)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
stearic acid (UNII: 4ELV7Z65AP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
totarol (UNII: 67NH2854WW)
BATILOL (UNII: 39YR661C4U)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
ARGININE (UNII: 94ZLA3W45F)
poloxamer 407 (UNII: TUF2IVW3M2)
polysorbate 80 (UNII: 6OZP39ZG8H)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
isododecane (UNII: A8289P68Y2)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
LAURYL TRISILOXANE (UNII: 5OHO78HI1D)
CITRUS PARADISI SEED (UNII: 12F08874Y7)
ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
octanediol (UNII: 806K32R50Z)
ethylhexylglycerin (UNII: 147D247K3P)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
polysorbate 20 (UNII: 7T1F30V5YH)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
ACEGLUTAMIDE (UNII: 01J18G9G97)
NEPIDERMIN (UNII: TZK30RF92W)
MECASERMIN (UNII: 7GR9I2683O)
BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)
FIBROBLAST GROWTH FACTOR-1 (UNII: G53298VN9Y)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69579-103-02	1 in 1 CARTON
1	NDC: 69579-103-01	30 mL in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/26/2015

Labeler - Phytos Co., Ltd. (689196775)

Registrant - Phytos Co., Ltd. (689196775)

Establishment
Name	Address	ID/FEI	Business Operations
Phytos Co., Ltd.		689196775	manufacture(69579-103)