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    NDC 61477-0211-26 ALOE UP PRO 50 3; 10; 5; 2.75; 4 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL Details

    ALOE UP PRO 50 3; 10; 5; 2.75; 4 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL

    ALOE UP PRO 50 is a TOPICAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Aloe Care International, LLC. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE.

    Product Information

    NDC 61477-0211
    Product ID 61477-211_dc9415f3-f8eb-8346-e053-2a95a90a9a3e
    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 PRO 50
    Proprietary Name Suffix CONTINUOUS SUNSCREEN
    Non-Proprietary Name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
    Product Type HUMAN OTC DRUG
    Dosage Form SPRAY
    Route TOPICAL
    Active Ingredient Strength 3; 10; 5; 2.75; 4
    Active Ingredient Units g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
    Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
    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 61477-0211-26 (61477021126)

    NDC Package Code 61477-211-26
    Billing NDC 61477021126
    Package 177 mL in 1 CAN (61477-211-26)
    Marketing Start Date 2014-02-24
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL dc33d9e8-3463-485d-a1ee-6319ed91454c Details

    Revised: 4/2022