Drugplain

NDC 17089-476-20

GUNA HAY FEVER RELIEF 200 [hp_X]/4g

strychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca flowering top - sulfur - · PELLET

No Recall History

GUNA HAY FEVER RELIEF is a pellet containing strychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca flowering top - sulfur - at a strength of 200 [hp_X]/4g. Manufactured by Guna spa.

Key Facts

Brand Name
GUNA HAY FEVER RELIEF
Generic Name
strychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca flowering top - sulfur -
NDC Code (Package)
17089-476-20
NDC Code (Product)
17089-476
Manufacturer
Guna spa
Strength
200 [hp_X]/4g
Dosage Form
PELLET
Route
ORAL
Marketing Status
Drug Class
Standardized Insect Venom Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]
Marketing Start
02/17/2021

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.