NDC 66096-527

OHM Sinus Nasal

Aralia Rac, Euphorbium, Galphimia, Hepar Sulph Calc, Histaminum, Hydrastis, Kali Bic, Kali Iod, Luffa, Pulsatilla, Teucrium Mar.

OHM Sinus Nasal is a Nasal Spray in the Human Otc Drug category. It is labeled and distributed by Ohm Pharma Inc.. The primary component is Aralia Racemosa Root; Euphorbia Resinifera Resin; Galphimia Glauca Flowering Top; Calcium Sulfide; Histamine Dihydrochloride; Goldenseal; Potassium Dichromate; Potassium Iodide; Luffa Operculata Fruit; Anemone Pulsatilla; Teucrium Marum.

Product ID66096-527_b8a6aed9-a175-f172-e053-2995a90a17a0
NDC66096-527
Product TypeHuman Otc Drug
Proprietary NameOHM Sinus Nasal
Generic NameAralia Rac, Euphorbium, Galphimia, Hepar Sulph Calc, Histaminum, Hydrastis, Kali Bic, Kali Iod, Luffa, Pulsatilla, Teucrium Mar.
Dosage FormSpray
Route of AdministrationNASAL
Marketing Start Date2017-01-23
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameOHM PHARMA INC.
Substance NameARALIA RACEMOSA ROOT; EUPHORBIA RESINIFERA RESIN; GALPHIMIA GLAUCA FLOWERING TOP; CALCIUM SULFIDE; HISTAMINE DIHYDROCHLORIDE; GOLDENSEAL; POTASSIUM DICHROMATE; POTASSIUM IODIDE; LUFFA OPERCULATA FRUIT; ANEMONE PULSATILLA; TEUCRIUM MARUM
Active Ingredient Strength6 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 66096-527-09

30 mL in 1 BOTTLE, SPRAY (66096-527-09)
Marketing Start Date2017-01-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 66096-527-09 [66096052709]

OHM Sinus Nasal SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-23

Drug Details

Active Ingredients

IngredientStrength
ARALIA RACEMOSA ROOT6 [hp_X]/30mL

OpenFDA Data

SPL SET ID:2aa6f339-3fe1-4f25-ad50-7e0b3536aa50
Manufacturer
UNII
UPC Code
  • 0366096527099

  • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.