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    NDC 61480-0310-01 DANDRUFF 3; 3; 1; 1; 1; 1; 1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 Details

    DANDRUFF 3; 3; 1; 1; 1; 1; 1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

    DANDRUFF is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by PLYMOUTH HEALTHCARE PRODUCTS LLC. The primary component is NICKEL SULFATE HEXAHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM BROMIDE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SODIUM CHLORIDE; SULFUR.

    Product Information

    NDC 61480-0310
    Product ID 61480-310_d44a68e4-354a-6192-e053-2a95a90a49a8
    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 DANDRUFF
    Proprietary Name Suffix n/a
    Non-Proprietary Name Kali Bromatum, Kali Muriaticum, Kali Sulphuricum, Natrum Muriaticum, Sulphur, Calcarea Carbonica, Niccolum Sulphuricum.
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 3; 3; 1; 1; 1; 1; 1
    Active Ingredient Units [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
    Substance Name NICKEL SULFATE HEXAHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM BROMIDE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SODIUM CHLORIDE; SULFUR
    Labeler Name PLYMOUTH HEALTHCARE PRODUCTS LLC
    Pharmaceutical Class Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA],
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 61480-0310-01 (61480031001)

    NDC Package Code 61480-310-01
    Billing NDC 61480031001
    Package 144 TABLET in 1 BOTTLE, PLASTIC (61480-310-01)
    Marketing Start Date 2017-05-24
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 212d6cbd-046d-40a5-b7dd-51b59d30b201 Details

    Revised: 12/2021