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    NDC 62032-0107-90 Obagi-C Rx System C-Sunguard 75; 90 mg/mL; mg/mL Details

    Obagi-C Rx System C-Sunguard 75; 90 mg/mL; mg/mL

    Obagi-C Rx System C-Sunguard is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by OMP, Inc.. The primary component is OCTINOXATE; ZINC OXIDE.

    Product Information

    NDC 62032-0107
    Product ID 62032-107_2bd2d38d-ac03-427e-a64c-4ececadae8ad
    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 Obagi-C Rx System C-Sunguard
    Proprietary Name Suffix SPF 30
    Non-Proprietary Name OCTINOXATE and ZINC OXIDE
    Product Type HUMAN OTC DRUG
    Dosage Form CREAM
    Route TOPICAL
    Active Ingredient Strength 75; 90
    Active Ingredient Units mg/mL; mg/mL
    Substance Name OCTINOXATE; ZINC OXIDE
    Labeler Name OMP, Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part352
    Listing Certified Through 2022-12-31

    Package

    NDC 62032-0107-90 (62032010790)

    NDC Package Code 62032-107-90
    Billing NDC 62032010790
    Package 1 BOTTLE, PLASTIC in 1 CARTON (62032-107-90) / 90 mL in 1 BOTTLE, PLASTIC
    Marketing Start Date 2002-01-01
    NDC Exclude Flag N
    Pricing Information N/A
    << 62032-0106-10 62032-0116-36 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 7b4aa8b4-124c-4e26-9a0a-d200867c3d11 Details

    Revised: 9/2019
    Document Id: 2bd2d38d-ac03-427e-a64c-4ececadae8ad
    Set id: 7b4aa8b4-124c-4e26-9a0a-d200867c3d11
    Version: 4
    Effective Time: 20190917