Label: ALLANTOIN- advanced derma spray aerosol, spray

  • Category: HUMAN OTC DRUG LABEL

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 February 12, 2018

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active ingredient

    Allantoin 0.5%

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  • Purpose

    Skin Protectant

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  • ​Uses

    Temporarily protects and helps relieve chapped or cracked skin

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  • Warnings

    For external use only.

    Contents under pressure. Do not puncture or incinerate. Do not store above 120 °F. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

    Do not use

    • on deep or puncture wounds
    • on animal bites
    • on serious burns

    When using this product

    • avoid spraying in eyes

    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

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

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  • Directions

    • shake well before using
    • apply as needed
    • spray product onto affected area(s) and massage into skin in a circular motion
    • for scars on face or near eyes spray product into palm of hand and apply with fingertips
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  • Other information

    store at room temperature

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  • Inactive ingredients

    Water, Dimethyl Ether, Isostearyl Isostearate, Isopropyl Isostearate, PPG-3 Benzyl Ether Myristate, Pentaerythrityl Tetracaprylate/Caprate, Methylsilanol Hydroxyproline Aspartate, Glycerin, Butylene Glycol, Allium Cepa (Onion) Bulb Extract, Sucrose Palmitate, Glyceryl Stearate, Glyceryl Stearate Citrate, Sucrose, Mannan, Xanthan Gum, Cetyl Hydroxyethylcellulose, Rutin, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Phaseolus Lunatus (Green Bean) SEed Extract, Phenoxyethanol, Fragrance, Potassium Sorbate, Salicylic Acid

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  • Questions?

    Call 1-866-964-0939

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  • Principal Display Panel

    Kroger

    Advanced Derma Spray

    Dermatologist Tested

    Allantoin 0.5% - Skin Protectant

    • Improves overall appearance of SCARS*
    • Improves the appearance of texture & smoothness on STRETCH MARKS*
    • Paraben Free

    Shake well before use.

    Net WT 3 OZ (85 g)

    Kroger_Advanced Derma Spray_50-126KR.jpg

    Kroger_Advanced Derma Spray_50-126KR.jpg

    Kroger_Advanced Derma Spray_50-126KR.jpg

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  • INGREDIENTS AND APPEARANCE
    ALLANTOIN 
    advanced derma spray aerosol, spray
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-195
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.425 g  in 85 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    DIMETHYL ETHER (UNII: AM13FS69BX)  
    ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)  
    PPG-3 BENZYL ETHER MYRISTATE (UNII: 8075L58MKO)  
    PENTAERYTHRITYL TETRACAPRYLATE/TETRACAPRATE (UNII: 832C4KF14X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ONION (UNII: 492225Q21H)  
    SUCROSE PALMITATE (UNII: 3OSQ643ZK5)  
    GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)  
    SUCROSE (UNII: C151H8M554)  
    YEAST MANNAN (UNII: 91R887N59P)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)  
    RUTIN (UNII: 5G06TVY3R7)  
    PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)  
    PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)  
    LIMA BEAN (UNII: 112YH1ZMX2)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:30142-195-85 85 g in 1 CAN; Type 0: Not a Combination Product 02/12/2018
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 02/12/2018
    Labeler - Kroger Co. (006999528)
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