Search by Drug Name or NDC

    NDC 49035-0944-24 equate hemorrhoidal 14.4; 15; .25; 1 g/100g; g/100g; g/100g; g/100g Details

    equate hemorrhoidal 14.4; 15; .25; 1 g/100g; g/100g; g/100g; g/100g

    equate hemorrhoidal is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Wal-Mart Stores Inc. The primary component is GLYCERIN; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE.

    Product Information

    NDC 49035-0944
    Product ID 49035-944_74326085-ef80-4c8e-a726-c528ff0a6ee6
    Associated GPIs 89992004743720
    GCN Sequence Number 061414
    GCN Sequence Number Description phenyleph/pramoxin/glycr/w.pet CREAM (G) 0.25%-1% RECTAL
    HIC3 Q3D
    HIC3 Description HEMORRHOIDAL PREPARATIONS
    GCN 97205
    HICL Sequence Number 034011
    HICL Sequence Number Description PHENYLEPHRINE HCL/PRAMOXINE HCL/GLYCERIN/WHITE PETROLATUM
    Brand/Generic Generic
    Proprietary Name equate hemorrhoidal
    Proprietary Name Suffix n/a
    Non-Proprietary Name glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum
    Product Type HUMAN OTC DRUG
    Dosage Form CREAM
    Route TOPICAL
    Active Ingredient Strength 14.4; 15; .25; 1
    Active Ingredient Units g/100g; g/100g; g/100g; g/100g
    Substance Name GLYCERIN; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE
    Labeler Name Wal-Mart Stores Inc
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC], alpha-1 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part346
    Listing Certified Through 2024-12-31

    Package

    NDC 49035-0944-24 (49035094424)

    NDC Package Code 49035-944-24
    Billing NDC 49035094424
    Package 1 TUBE in 1 CARTON (49035-944-24) / 51 g in 1 TUBE
    Marketing Start Date 2007-09-25
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 5ccefdbd-bbbe-4cbf-9fdb-3c568643e14d Details

    Revised: 1/2019