NDC 59824-0008

PainMed Homeopathic Pain Relieving External

Aconitum Napellus, Arnica Montana, Bellis Perennis, Bryonia Alba Root, Calendula Officinalis Flowering Top, Hamamelis Virginiana Root Bark/stem Bark, Hypericum Perforatum, Ledum Palustre Twig, And Ruta Graveolens Flowering Top

PainMed Homeopathic Pain Relieving External is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by G M International, Inc.. The primary component is Aconitum Napellus; Arnica Montana; Bellis Perennis; Bryonia Alba Root; Calendula Officinalis Flowering Top; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum; Rhododendron Tomentosum Leafy Twig; Ruta Graveolens Flowering Top.

Product ID59824-0008_bb7f3c11-acfb-4b01-829d-20d77054b54a
NDC59824-0008
Product TypeHuman Otc Drug
Proprietary NamePainMed Homeopathic Pain Relieving External
Generic NameAconitum Napellus, Arnica Montana, Bellis Perennis, Bryonia Alba Root, Calendula Officinalis Flowering Top, Hamamelis Virginiana Root Bark/stem Bark, Hypericum Perforatum, Ledum Palustre Twig, And Ruta Graveolens Flowering Top
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2003-08-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameG M International, Inc.
Substance NameACONITUM NAPELLUS; ARNICA MONTANA; BELLIS PERENNIS; BRYONIA ALBA ROOT; CALENDULA OFFICINALIS FLOWERING TOP; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HYPERICUM PERFORATUM; RHODODENDRON TOMENTOSUM LEAFY TWIG; RUTA GRAVEOLENS FLOWERING TOP
Active Ingredient Strength3 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 59824-0008-2

1 TUBE in 1 BOX (59824-0008-2) > 42.5 g in 1 TUBE
Marketing Start Date2003-08-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59824-0008-2 [59824000802]

PainMed Homeopathic Pain Relieving External GEL
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-08-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACONITUM NAPELLUS3 [hp_X]/g

OpenFDA Data

SPL SET ID:cf85b8db-ba3c-4478-9456-90d7adb65286
Manufacturer
UNII

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