Search by Drug Name or NDC

    NDC 67618-0165-01 Betadine Dry Powder 0.05 mg/mL Details

    Betadine Dry Powder 0.05 mg/mL

    Betadine Dry Powder is a TOPICAL AEROSOL, SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Atlantis Consumer Healthcare, Inc.. The primary component is POVIDONE-IODINE.

    Product Information

    NDC 67618-0165
    Product ID 67618-165_a3cb4462-d000-4159-bb26-678d8c7280c3
    Associated GPIs 92200040003340
    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 Betadine Dry Powder
    Proprietary Name Suffix n/a
    Non-Proprietary Name POVIDONE-IODINE
    Product Type HUMAN OTC DRUG
    Dosage Form AEROSOL, SPRAY
    Route TOPICAL
    Active Ingredient Strength 0.05
    Active Ingredient Units mg/mL
    Substance Name POVIDONE-IODINE
    Labeler Name Atlantis Consumer Healthcare, Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M003
    Listing Certified Through 2024-12-31

    Package

    NDC 67618-0165-01 (67618016501)

    NDC Package Code 67618-165-01
    Billing NDC 67618016501
    Package 56.7 mL in 1 CAN (67618-165-01)
    Marketing Start Date 2020-06-15
    NDC Exclude Flag N
    Pricing Information N/A
    << 67618-0160-03 67618-0180-12 >>

    Contents