Search by Drug Name or NDC

    NDC 61477-0221-14 ALOE UP COCO-MANGO 3; 15; 5; 15 g/100mL; g/100mL; g/100mL; g/100mL Details

    ALOE UP COCO-MANGO 3; 15; 5; 15 g/100mL; g/100mL; g/100mL; g/100mL

    ALOE UP COCO-MANGO is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by Aloe Care International, LLC. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE.

    Product Information

    NDC 61477-0221
    Product ID 61477-221_dc93da28-9f59-4361-e053-2995a90ad440
    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 ALOE UP COCO-MANGO
    Proprietary Name Suffix SPF-50
    Non-Proprietary Name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
    Product Type HUMAN OTC DRUG
    Dosage Form LOTION
    Route TOPICAL
    Active Ingredient Strength 3; 15; 5; 15
    Active Ingredient Units g/100mL; g/100mL; g/100mL; g/100mL
    Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
    Labeler Name Aloe Care International, LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part352
    Listing Certified Through 2023-12-31

    Package

    NDC 61477-0221-14 (61477022114)

    NDC Package Code 61477-221-14
    Billing NDC 61477022114
    Package 118 mL in 1 TUBE (61477-221-14)
    Marketing Start Date 2019-02-18
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 8506049f-cb43-4d1d-885b-c6d3a99bbba3 Details

    Revised: 4/2022