P1P MAGIC WHITENING ANTIAGING- niacinamide, panthenol, adenosine liquid

P1P Magic Whitening Antiaging by

Drug Labeling and Warnings

P1P Magic Whitening Antiaging by is a Otc medication manufactured, distributed, or labeled by Phytos Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

P1P Magic Whitening & Antiaging

Niacinamide (2.5%)Panthenol (1%) Adenosine (0.04%) 

skin protectant

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

Moisturizes skin

For 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 

DirectionsApply moderate amount gently on face after cleanse

Water, Cetyl Ethylhexanoate,Tranexamic Acid, Centella Asiatica Extract, Bacillus/Soybean Ferment Extract, Salix Alba (Willow) Bark Extract, Morus Alba Bark Extract, Paeonia Suffruticosa Root Extract, Camellia Sinensis Leaf Extract, Oligopeptide-1, Oligopeptide-2, Tremella Fuciformis Sporocarp Extract, Palmitoyl Oligopeptide, Glycosyl Trehalose, Lecithin, Glycerin, 3-O-Ethyl Ascorbic Acid, 1,2-Hexanediol, Panthenol, Tocopheryl Acetate, Polysorbate 80, Poloxamer 407, Dipotassium Glycyrrhizate, Citric Acid, Phytosphingosine Phosphate

INGREDIENTS AND APPEARANCE

P1P MAGIC WHITENING ANTIAGING 
niacinamide, panthenol, adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69579-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	niacinamide	0.025   in 30 mL
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z)	PANTHENOL	0.01   in 30 mL
adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	adenosine	0.0004   in 30 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
TRANEXAMIC ACID (UNII: 6T84R30KC1)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
SALIX ALBA BARK (UNII: 205MXS71H7)
morus alba bark (UNII: 7O71A48NDP)
PAEONIA SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
glycerin (UNII: PDC6A3C0OX)
3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POLOXAMER 407 (UNII: TUF2IVW3M2)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69579-105-02	1 in 1 CARTON
1	NDC: 69579-105-01	30 mL in 1 AMPULE

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(69579-105)