O HUI WHITE EXTREME CELLIGHT (PROTOCATECHUALDEHYDE) EMULSION [LG HOUSEHOLD AND HEALTHCARE, INC.]

O HUI WHITE EXTREME CELLIGHT (PROTOCATECHUALDEHYDE) EMULSION [LG HOUSEHOLD AND HEALTHCARE, INC.]
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NDC 53208-501-01, 53208-501-02
Set ID 47fa92f4-2993-4f27-9661-0bfa200f4b0f
Category HUMAN OTC DRUG LABEL
Packager LG Household and Healthcare, Inc.
Generic Name
Product Class
Product Number
Application Number
  • ACTIVE INGREDIENT

    PROTOCATECHUALDEHYDE 0.0315%
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  • PURPOSE

    Whitening Emulsion

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  • WARNINGS

    Stop use if rash or irritation develops and lasts. Close
  • WHEN USING

    Keep out of eyes. Rinse with water to remove.

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  • INDICATIONS & USAGE

    Use to whiten skin.

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. Is swallowed, get medical help or contact a Poison Control Center right away.

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  • INACTIVE INGREDIENT

    WATER, GLYCERIN, DIPROPYLENE GLYCOL, MEDIUM-CHAIN TRIGLYCERIDES, TRIETHYLHEXANOIN, HYDROGENATED POLYDECENE, CYCLOPENTASILOXANE, BETAINE, BIOSACCHARIDE GUM-1, ALCOHOL, GLYCERYL MONOSTEARATE, FRUIT, YELLOW WAX, STEARIC ACID, PANTHENOL, COPPER  TRIPEPTIDE-1, METHYLPARABEN, PROPYLPARABEN,  ETHYLPARABEN, XANTHAN GUM, SODIUM METABISULFITE, TRISODIUM EDTA, CITRIC ACID.

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  • PRINCIPAL DISPLAY PANEL

    OHUI

    WHITE EXTREME

    CELLIGHT EMULSION

    White Extreme EMulsion

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  • DOSAGE & ADMINISTRATION

    Use as needed to whiten skin.

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  • INGREDIENTS AND APPEARANCE
    O HUI WHITE EXTREME CELLIGHT 
    protocatechualdehyde emulsion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:53208-501
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PROTOCATECHUALDEHYDE (UNII: 4PVP2HCH4T) (PROTOCATECHUALDEHYDE - UNII:4PVP2HCH4T) PROTOCATECHUALDEHYDE 0.0315 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    FRUIT (UNII: C2AIY4ERZC)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    BETAINE (UNII: 3SCV180C9W)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    COPPER (UNII: 789U1901C5)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    EDETATE TRISODIUM (UNII: 420IP921MB)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:53208-501-02 1 in 1 BOX
    1 NDC:53208-501-01 150 mL in 1 CONTAINER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 03/07/2011
    Labeler - LG Household and Healthcare, Inc. (688276187)
    Registrant - LG Household and Healthcare, Inc. (688276187)
    Establishment
    Name Address ID/FEI Business Operations
    LG Household and Healthcare, Inc. 688276187 manufacture
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