NDC 62795-1134

Hendel Sinus Relief

Echinacea Purpurea,anemone Pulsatilla,eupatorium Perfoliatum Flowering,goldenseal,potassdichromate, Luffa Operculata Fruit, Potassium Iodide, Calcium Sulfide And Mercuric Sulfide

Hendel Sinus Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Medinatura Inc. The primary component is Echinacea Purpurea; Anemone Pulsatilla; Eupatorium Perfoliatum Flowering Top; Goldenseal; Potassium Dichromate; Luffa Operculata Fruit; Potassium Iodide; Calcium Sulfide; Mercuric Sulfide.

Product ID62795-1134_d3fd4dd0-2b01-4af1-98c6-13386c7a10b4
NDC62795-1134
Product TypeHuman Otc Drug
Proprietary NameHendel Sinus Relief
Generic NameEchinacea Purpurea,anemone Pulsatilla,eupatorium Perfoliatum Flowering,goldenseal,potassdichromate, Luffa Operculata Fruit, Potassium Iodide, Calcium Sulfide And Mercuric Sulfide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-06-22
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameMediNatura Inc
Substance NameECHINACEA PURPUREA; ANEMONE PULSATILLA; EUPATORIUM PERFOLIATUM FLOWERING TOP; GOLDENSEAL; POTASSIUM DICHROMATE; LUFFA OPERCULATA FRUIT; POTASSIUM IODIDE; CALCIUM SULFIDE; MERCURIC SULFIDE
Active Ingredient Strength3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 62795-1134-2

100 TABLET in 1 PACKAGE (62795-1134-2)
Marketing Start Date2016-06-22
Marketing End Date2027-04-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62795-1134-2 [62795113402]

Hendel Sinus Relief TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-22
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ECHINACEA PURPUREA3 [hp_X]/1

OpenFDA Data

SPL SET ID:819425a8-b4ec-4049-95cb-187f6729dde5
Manufacturer
UNII
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