Search by Drug Name or NDC

    NDC 62032-0413-20 Tretinoin 0.05 g/100g Details

    Tretinoin 0.05 g/100g

    Tretinoin is a TOPICAL GEL in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Obagi Cosmeceuticals LLC. The primary component is TRETINOIN.

    Product Information

    NDC 62032-0413
    Product ID 62032-413_6ab5cf57-07a1-4222-8ff5-3960206df180
    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 Tretinoin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Tretinoin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form GEL
    Route TOPICAL
    Active Ingredient Strength 0.05
    Active Ingredient Units g/100g
    Substance Name TRETINOIN
    Labeler Name Obagi Cosmeceuticals LLC
    Pharmaceutical Class Retinoid [EPC], Retinoids [CS]
    DEA Schedule n/a
    Marketing Category NDA AUTHORIZED GENERIC
    Application Number NDA022070
    Listing Certified Through 2024-12-31

    Package

    NDC 62032-0413-20 (62032041320)

    NDC Package Code 62032-413-20
    Billing NDC 62032041320
    Package 20 g in 1 TUBE (62032-413-20)
    Marketing Start Date 2014-06-19
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL c5ee36ac-2ffd-4cca-ad47-b1dae7ebdb3b Details

    Revised: 5/2021