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    NDC 10733-0412-60 lumicain 250 mg/g Details

    lumicain 250 mg/g

    lumicain is a TOPICAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Medical Products Laboratories, Inc.. The primary component is ALUMINUM CHLORIDE.

    Product Information

    NDC 10733-0412
    Product ID 10733-412_b725dd26-c793-51a4-e053-2a95a90a573d
    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 lumicain
    Proprietary Name Suffix n/a
    Non-Proprietary Name Aluminium Chloride Hexahydrate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route TOPICAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/g
    Substance Name ALUMINUM CHLORIDE
    Labeler Name Medical Products Laboratories, Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 10733-0412-60 (10733041260)

    NDC Package Code 10733-412-60
    Billing NDC 10733041260
    Package 67 g in 1 BOTTLE (10733-412-60)
    Marketing Start Date 2020-09-29
    NDC Exclude Flag N
    Pricing Information N/A
    << 10733-0176-01 10733-0415-40 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 9fdcce3e-e4d4-41ae-8609-37987c12414e Details

    Revised: 12/2020
    Document Id: b725dd26-c793-51a4-e053-2a95a90a573d
    Set id: 9fdcce3e-e4d4-41ae-8609-37987c12414e
    Version: 4
    Effective Time: 20201223