NDC | 69579-105-01, 69579-105-02 |
Set ID | c394d622-8af6-4b11-b762-7a76af509b31 |
Category | HUMAN OTC DRUG LABEL |
Packager | Phytos Co., Ltd. |
Generic Name | |
Product Class | Adenosine Receptor Agonist |
Product Number | |
Application Number |
- 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
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INGREDIENTS AND APPEARANCE
P1P MAGIC WHITENING ANTIAGING
niacinamide, panthenol, adenosine liquidProduct 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)