NDC 43406-0709

Hemorrhoid Gel

Achillea Millefolium, Aesculus Hippocastanum, Hamamelis Virginiana, Ruscus Aculeatus, Aloe Socotrina, Paeonia Officinalis, Ignatia Amara, Nitricum Acidum, Nux Vomica, Phosphorus, Podophyllum Peitatum, Pulsatilla, Ratanhia, Chelidonium Majus, Sulphur

Hemorrhoid Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Natural Creations, Inc. The primary component is Achillea Millefolium Whole; Aloe; Chelidonium Majus Whole; Hamamelis Virginiana Root Bark/stem Bark; Horse Chestnut; Krameria Lappacea Root; Nitric Acid; Paeonia Officinalis Root; Phosphorus; Podophyllum; Pulsatilla Vulgaris Whole; Ruscus Aculeatus Whole; Strychnos Ignatii Seed; Strychnos Nux-vomica Seed; Sulfur.

Product ID43406-0709_a515d3ae-7a24-45b9-9bcf-a3ec565cd89c
NDC43406-0709
Product TypeHuman Otc Drug
Proprietary NameHemorrhoid Gel
Generic NameAchillea Millefolium, Aesculus Hippocastanum, Hamamelis Virginiana, Ruscus Aculeatus, Aloe Socotrina, Paeonia Officinalis, Ignatia Amara, Nitricum Acidum, Nux Vomica, Phosphorus, Podophyllum Peitatum, Pulsatilla, Ratanhia, Chelidonium Majus, Sulphur
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2019-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameNatural Creations, Inc
Substance NameACHILLEA MILLEFOLIUM WHOLE; ALOE; CHELIDONIUM MAJUS WHOLE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HORSE CHESTNUT; KRAMERIA LAPPACEA ROOT; NITRIC ACID; PAEONIA OFFICINALIS ROOT; PHOSPHORUS; PODOPHYLLUM; PULSATILLA VULGARIS WHOLE; RUSCUS ACULEATUS WHOLE; STRYCHNOS IGNATII SEED; STRYCHNOS NUX-VOMICA SEED; SULFUR
Active Ingredient Strength4 [hp_X]/g; [hp_X]/g; [hp_C]/g; [hp_X]/g; [hp_C]/g; [hp_C]/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; [hp_C]/g
Pharm ClassesAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC Exclude FlagN
Listing Certified Through2024-12-31

Packaging

NDC 43406-0709-5

56.7 g in 1 TUBE, WITH APPLICATOR (43406-0709-5)
Marketing Start Date2019-09-12
NDC Exclude FlagN
Sample Package?N

Drug Details


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