Label: BARUBT UREA MOISTURIZING CREAM- urea moisturizing cream cream

  • NDC Code(s): 84712-022-01
  • Packager: Guangdong Youbaijia Cosmetic Industry Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 18, 2024

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  • ACTIVE INGREDIENT

    OLEA EUROPAEA FRUIT OIL 2%
    JOJOBA(SIMMONDSIA CHINENSIS)SEED OIL 2%
    SALICYLIC ACID 2%

  • INACTIVE INGREDIENT

    UREA, MINERAL OIL,MINERAL GREASE, EARTH WAX, WHITE BEESWAX, ETHYL HEXYL PALMITATE,BUTYROSPERMUM PARKII FRUIT FAT, ALOE VERA IN CURACAO BARBADENSIS EXTRACT, (DAILY)ESSENCE, HYDROXYPHENYL PROPYL ESTER, C1 19140.

  • DO NOT USE

    Do not use on damaged skin.

  • KEEP OUT OF REACH OF CHILDREN

    Keep away from children. Do not swallow.

  • PURPOSE

    Moisturizing& Nourishing Hand & Foot Skin

  • QUESTIONS

    Contact name: Jessie Peng
    Company phone number: +1 818 579 7288
    Company e-mail: jessie@registeragentllc.com

  • STOP USE

    lf skin becomes red or irritated, discontinue use immediately and wash with water.

  • WHEN USING

    keep out of eyes. Rinse with water to remove.

  • WARNINGS

    For external use only.

  • STORAGE AND HANDLING

    Keep away from light and in a dry place.

  • INDICATIONS & USAGE

    CONTAINS A VARIETY OF MOISTURIZING EXTRACTS,FRESH AND MOISTURIZING TEXTURE; EFFECTIVELY MOISTURIZE,SOFTEN DRY AND CHAPPED SKIN, MAINTAIN SKIN MOISTURE; MOISTURIZE THE HANDS, FEET AND OTHER SKIN, SO THAT THE SKIN IS MOISTURIZED AND SMOOTH.IT IMPROVES ROUGHNESS OF THE SKIN AND MAKES THE SKIN SMOOTH AND SOFT.HAT THE SKIN IS MOIST AND SMOOTH.

  • DOSAGE & ADMINISTRATION

    Apply the moisturizer to the skin before bed or after bathing and massage in circular motions to absorb. For better results, it is recommended to use 2-3 times a week.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    BARUBT UREA MOISTURIZING CREAM 
    urea moisturizing cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84712-022
    Route of AdministrationCUTANEOUS, TOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.8 g  in 40 g
    OLEA EUROPAEA FRUIT VOLATILE OIL (UNII: 8E7358CX1J) (OLEA EUROPAEA FRUIT VOLATILE OIL - UNII:8E7358CX1J) OLEA EUROPAEA FRUIT VOLATILE OIL0.8 g  in 40 g
    SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) (SIMMONDSIA CHINENSIS SEED - UNII:D24K2Q1F6H) SIMMONDSIA CHINENSIS SEED0.8 g  in 40 g
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP) 5.14 g  in 40 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84712-022-0140 g in 1 BOTTLE; Type 0: Not a Combination Product09/17/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01609/17/2024
    Labeler - Guangdong Youbaijia Cosmetic Industry Co., Ltd (702314361)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Youbaijia Cosmetic Industry Co., Ltd702314361label(84712-022) , manufacture(84712-022)
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