NDC 17089-476 – Guna Hay Fever Relief

Strychnos Nux-vomica Seed 4 [hp_X]/4g; Histamine Dihydrochloride 200 [hp_X]/4g; Manganese 8 [hp_X]/4g; Schoenocaulon Officinale Seed 6 [hp_X]/4g; Onion 30… · Pellet · Oral

Human Otc Drug

Product NDC17089-476

Product details

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 -
Labeler
Guna spa
Dosage form
Pellet
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
February 17, 2021
Listing expires
December 31, 2026
Pharmacologic class
Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Standardized Insect Venom Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Guna Hay Fever Relief →

Package NDC codes (2)

Package NDCDescriptionSince
17089-476-202 TUBE in 1 BOX (17089-476-20) / 4 g in 1 TUBEFeb 17, 2021
17089-476-211 TUBE in 1 BOX (17089-476-21) / 4 g in 1 TUBEDec 15, 2021