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    NDC 70116-0011-01 Eezysun Aloe Vera After Sun .1; .1; .5; .3; .4; .15 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL Details

    Eezysun Aloe Vera After Sun .1; .1; .5; .3; .4; .15 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL

    Eezysun Aloe Vera After Sun is a TOPICAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by BIO EARTH MANUFACTURING (PTY) LTD. The primary component is ANIBA ROSAEODORA WHOLE; CALENDULA OFFICINALIS FLOWERING TOP; HYALURONIC ACID; LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER; MATRICARIA CHAMOMILLA WHOLE; MENTHA X PIPERITA WHOLE.

    Product Information

    NDC 70116-0011
    Product ID 70116-011_080481fe-6394-0252-e063-6294a90a3b13
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Eezysun Aloe Vera After Sun
    Proprietary Name Suffix n/a
    Non-Proprietary Name Aniba Rosaedora, Calendula Officinails, Hyaluronic Acid, Lavandula Officinalis, Matricaria Chamomilla, Mentha Piperita
    Product Type HUMAN OTC DRUG
    Dosage Form GEL
    Route TOPICAL
    Active Ingredient Strength .1; .1; .5; .3; .4; .15
    Active Ingredient Units g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
    Substance Name ANIBA ROSAEODORA WHOLE; CALENDULA OFFICINALIS FLOWERING TOP; HYALURONIC ACID; LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER; MATRICARIA CHAMOMILLA WHOLE; MENTHA X PIPERITA WHOLE
    Labeler Name BIO EARTH MANUFACTURING (PTY) LTD
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 70116-0011-01 (70116001101)

    NDC Package Code 70116-011-01
    Billing NDC 70116001101
    Package 100 mL in 1 TUBE (70116-011-01)
    Marketing Start Date 2021-03-26
    NDC Exclude Flag N
    Pricing Information N/A