Label: P1P MAGIC WHITENING ANTIAGING- niacinamide, panthenol, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69579-105-01, 69579-105-02 - Packager: Phytos Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated February 10, 2015
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- Official Label (Printer Friendly)
- 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)