W-CARE (ALLANTOIN) GEL [LAVIOR INC.]

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W-CARE (ALLANTOIN) GEL [LAVIOR INC.]
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NDC 71521-876-30
Set ID 55a9859c-e564-487d-e054-00144ff88e88
Category HUMAN OTC DRUG LABEL
Packager Lavior Inc.
Generic Name
Product Class
Product Number
Application Number PART347
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  • Active ingredient:

    Allantoin 0.5%..........................skin protectatant

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  • Purpose:

    skin protectant

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  • Uses:

    • helps prevent and relieve dry, chafed, chapped, or cracked skin
    • temporarily protects minor cuts, scrapes, and burns
    • helps protect from the drying effects of wind and cold weather
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  • Warnings:

    For external use only

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  • WHEN USING

    When using this product

    • avoid contact with eyes
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  • ASK DOCTOR

    Stop use and ask a doctor if

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days
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  • DO NOT USE


    Do not use on

    • deep or puncture wounds
    • animal bites
    • serious burns
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  • KEEP OUT OF REACH OF CHILDREN

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

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  • Directions

    • apply a thin layer 1 to 2 times daily, or as directed by a doctor
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  • Other information

    • store at room temperature
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  • Inactive ingredients:

    Aqua, Glycerin, Inula Viscosa Flower/Leaf/Stem Extract, Aloe Barbadensis Leaf Juice, Xanthan Gum, Sodium Benzoate, Potassium Sorbate, Citric Acid, Tocopheryl Acetate (Vitamin E), Sodium Hyaluronate

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  • Questions?

    Call toll free 1844-474-2552 or visit www.lavior.com

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  • INGREDIENTS AND APPEARANCE
    W-CARE 
    allantoin gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:71521-876
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.5 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    DITTRICHIA VISCOSA WHOLE (UNII: 3SYW69FH88)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:71521-876-30 1 in 1 BOX 07/31/2017
    1 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 07/31/2017
    Labeler - Lavior Inc. (080685327)
    Establishment
    Name Address ID/FEI Business Operations
    Lavior Inc. 080685327 manufacture(71521-876)
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