Label: RICE RAW PULP FACE CREAM ADDED RICE EXTRACT cream

  • NDC Code(s): 83872-126-01
  • Packager: Shenzhen XiaoMai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 2, 2024

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

View All Sections
  • ACTIVE INGREDIENT

    Oryza Sativa (Rice) Extract: 5.0%
    Glycerin: 5.0%

  • PURPOSE

    Water: 70.0%
    Cetyl Alcohol: 3.0%
    Caprylic/Capric Triglyceride: 5.0%
    Cyclohexasiloxane: 4.0%
    Propylene Glycol: 3.0%
    Mineral Oil: 3.0%
    Oleic Acid Glycerides: 1.0%
    Caprylyl Glycol: 1.0%

  • Uses

    Suitable for daily facial care to promote smoother and softeskin.

  • WARNINGS

    For external use only. Avoid contact with eyes and mucous membranes.

  • Do not use


    on damaged or broken skin.

  • When using this product

    keep out of eyes.
    Rinse with water to remove.

  • Stop use and ask a doctor

    Discontinue use if irritation occurs.

  • Keep out of reach of children.

    Keep out of reach of children.

  • Directions for use

    1.Apply the cream evenly to clean face and neck.
    2. Gently massage until fully absorbed.

  • INACTIVE INGREDIENT

    Water: 70.0%
    Cetyl Alcohol: 3.0%
    Caprylic/Capric Triglyceride: 5.0%
    Cyclohexasiloxane: 4.0%
    Propylene Glycol: 3.0%
    Mineral Oil: 3.0%
    Oleic Acid Glycerides: 1.0%
    Caprylyl Glycol: 1.0%

  • Other Information

    Store in a cool, dry place away from direct sunlight and heat.
    Keep packaging intact.

  • PRINCIPAL DISPLAY PANEL

    9

  • INGREDIENTS AND APPEARANCE
    RICE RAW PULP FACE CREAM ADDED RICE EXTRACT 
    rice raw pulp face cream added rice extract cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-126
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP) 30 mg  in 1 g
    WATER (UNII: 059QF0KO0R) 700 mg  in 1 g
    CETYL ALCOHOL (UNII: 936JST6JCN) 30 mg  in 1 g
    CAPRYLYL GLYCOL (UNII: 00YIU5438U) 10 mg  in 1 g
    OLEIC ACID (UNII: 2UMI9U37CP) 10 mg  in 1 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-126-0150 g in 1 BOTTLE; Type 0: Not a Combination Product05/02/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01605/02/2024
    Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen XiaoMai Manufacturing Co., Ltd.712999147manufacture(83872-126)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!