Label: MOIST MOISTURE BB- titanium dioxide, zinc oxide, octinoxate cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 10, 2018

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active Ingredients: Titanium Dioxide 7%, Zinc Oxide 7%, Ethylhexyl Methoxycinnamate 7%

  • INACTIVE INGREDIENT

    Inactive Ingredients:
    Water,Cyclopentasiloxane,Cyclohexasiloxane,Glycerin,Butylene Glycol Dicaprylate/Dicaprate, Phenyl Trimethicone,Mica (CI 77019),Cetyl PEG/PPG-10/1 Dimethicone,Arbutin,Pentylene Glycol,Talc,Dicaprylyl Carbonate,Caprylyl Methicone,Disteardimonium Hectorite,Sodium Chloride,Butylene Glycol,Sorbitan Isostearate,Tribehenin,Hexyl Laurate,Ceresin,Iron Oxides (CI 77492),Snail Secretion Filtrate,Dimethicone,Phenoxyethanol,Dimethicone Crosspolymer, Fragrance(Parfum),Iron Oxides (CI 77491),Iron Oxides (CI 77499),Ethylhexylglycerin, Hydrogenated Castor Oil Isostearate,Adenosine,Disodium EDTA,Triethoxycaprylylsilane,Ethyl Hexanediol,Helianthus Annuus (Sunflower) Seed Oil,Centella Asiatica Extract,Glycyrrhiza Glabra (Licorice) Root Extract,Angelica
    Gigas Root Extract,Scutellaria Baicalensis Root Extract, Chrysanthemum Morifolium Flower Extract,Eucommia Ulmoides Extract,Ophiopogon Japonicus Root Extract,Artemisia Princeps Leaf Extract,Cnidium Officinale Root Extract, Gardenia Florida Fruit Extract, Polygonum Multiflorum Root Extract, Carthamus Tinctorius (Safflower) Flower Extract,Astragalus Membranaceus Root Extract,Coptis Chinensis Root Extract,Phellodendron Amurense Bark Extract,Cassia Angustifolia Seed Polysaccharide, Portulaca Oleracea Extract,Origanum Vulgare Leaf Extract,Salix Alba (Willow) Bark Extract, Chamaecyparis Obtusa Leaf Extract, Cinnamomum Cassia Bark Extract,Lactobacillus/Soybean Ferment Extract

  • PURPOSE

    Purpose: Sunscreen

  • WARNINGS

    Warning:
    1. In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist.
    1) In case of having problems such as red rash, swollenness, itching, stimulation during usage.
    2) In case of having the same symptoms above on the part you put this product on by direct sunlight.
    2. you are banned to use it on the part where you have a scar, eczema, or dermatitis.
    3. In case of getting it into your eyes, you have to wash it immediately.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS AND USAGE

    Indication and Usage: After skincare, apply appropriate amount on all over the face.

  • DOSAGE AND ADMINISTRATION

    Dosage and Administration : Take an adequate amount of this product.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    MOIST MOISTURE BB 
    titanium dioxide, zinc oxide, octinoxate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69072-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) Titanium Dioxide3.5 mg  in 50 mL
    Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION3.5 mg  in 50 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE3.5 mg  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69072-010-0150 mL in 1 CARTON; Type 0: Not a Combination Product06/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35206/01/2014
    Labeler - Seindni Co.,ltd (557837682)
    Registrant - Seindni Co.,ltd (557837682)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosmax, Inc.689049693manufacture(69072-010)