Label: MISSHA M PERFECT COVER BB NO 13- zinc oxide, titanium dioxide, octinoxate cream
- NDC Code(s): 13733-141-01, 13733-141-02, 13733-141-03
- Packager: Able C&C Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 4, 2024
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- Active Ingredient
- Purpose
- Uses
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Directions
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water-resistant sunscreen if swimming or sweating
Sun protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regulary use a sunscreen with SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats and sunglasses
- Other Information
- Questions or comments?
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INACTIVE INGREDIENT
Water, Cyclopentasiloxane, Propylene Glycol, Caprylic/Capric Triglyceride, PEG-10 Dimethicone, Glycerin, Cetyl PEG/PPG-10/1 Dimethicone, Arbutin, Mineral Oil, Polyethylene, Talc, Phenyl Trimethicone, Beeswax (Cera Alba), Sodium Chloride, Ferric Oxide Yellow, Methylparaben, Dimethicone, Ferric Oxide Red, Propylparaben, Rosa Canina Fruit Oil, Squalane, Macadamia Ternifolia Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Cyclotetrasiloxane, Ferrosoferric oxide, Disodium EDTA, Adenosine, Algae Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Ceramide NP, Butylene Glycol, Fagus Sylvatica Bud Extract, Hydrolyzed collagen, Caprylyl Glycol, Benzyl Alcohol, 1,2-Hexanediol, Caprylhydroxamic Acid, Tocopherol, Benzoic Acid, Sodium Hyaluronate, Phenoxyethanol, Tropolone, Fragrance (Parfum), Butylphenyl Methylpropional, Benzyl Salicylate, Hydroxycitronellal, Alpha-Isomethyl Ionone, Hexyl Cinnamal, Linalool, Citronellol, Limonene
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MISSHA M PERFECT COVER BB NO 13
zinc oxide, titanium dioxide, octinoxate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:13733-141 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 0.07 g in 1 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.0419 g in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 0.075 g in 1 g Inactive Ingredients Ingredient Name Strength MACADAMIA OIL (UNII: 515610SU8C) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CERAMIDE 6 II (UNII: F1X8L2B00J) FAGUS SYLVATICA FLOWER BUD (UNII: 6D5V13045W) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) TOCOPHEROL (UNII: R0ZB2556P8) BENZOIC ACID (UNII: 8SKN0B0MIM) HYALURONATE SODIUM (UNII: YSE9PPT4TH) TROPOLONE (UNII: 7L6DL16P1T) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) WATER (UNII: 059QF0KO0R) CYCLOMETHICONE (UNII: NMQ347994Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) TALC (UNII: 7SEV7J4R1U) SODIUM CHLORIDE (UNII: 451W47IQ8X) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) METHYLPARABEN (UNII: A2I8C7HI9T) FERRIC OXIDE RED (UNII: 1K09F3G675) SQUALANE (UNII: GW89575KF9) ARBUTIN (UNII: C5INA23HXF) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) ABRONIA VILLOSA LEAF (UNII: A138B5260A) YELLOW WAX (UNII: 2ZA36H0S2V) DIMETHICONE (UNII: 92RU3N3Y1O) PROPYLPARABEN (UNII: Z8IX2SC1OH) LAMINARIA HYPERBOREA (UNII: NXA595GQ1K) ROSEMARY (UNII: IJ67X351P9) BENZYL ALCOHOL (UNII: LKG8494WBH) CYCLOMETHICONE 4 (UNII: CZ227117JE) JOJOBA OIL (UNII: 724GKU717M) FERROSOFERRIC OXIDE (UNII: XM0M87F357) ADENOSINE (UNII: K72T3FS567) CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9) MINERAL OIL (UNII: T5L8T28FGP) TRIS(TRIMETHYLSILOXY)PHENYLSILANE (UNII: S3QI0ZXT5X) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13733-141-01 50 g in 1 TUBE; Type 0: Not a Combination Product 10/01/2019 2 NDC:13733-141-02 20 g in 1 TUBE; Type 0: Not a Combination Product 10/01/2019 3 NDC:13733-141-03 1 g in 1 PACKET; Type 0: Not a Combination Product 10/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/01/2019 Labeler - Able C&C Co., Ltd. (689540284) Registrant - Able C&C Co., Ltd. (689540284) Establishment Name Address ID/FEI Business Operations Hanacos Co., Ltd. 690177857 manufacture(13733-141)