NDC 17089-476

GUNA HAY FEVER RELIEF

Strychnos Nux Vomica Seed - Histamine Dihydrochloride - Manganese - Schoenocaulon Officinale Seed - Apis Mellifera - Arsenic Trioxide - Silver Nitrate - Onion - Euphrasia Stricta - Galphimia Glauca Flowering Top - Sulfur -

GUNA HAY FEVER RELIEF is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Strychnos Nux-vomica Seed; Histamine Dihydrochloride; Manganese; Schoenocaulon Officinale Seed; Apis Mellifera; Silver Nitrate; Onion; Euphrasia Stricta; Galphimia Glauca Flowering Top; Sulfur; Arsenic Trioxide.

• Product ID: 17089-476_b8db510a-9908-6f15-e053-2a95a90a432c
• NDC: 17089-476
• Product Type: Human Otc Drug
• Proprietary 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 -
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2021-02-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Guna spa
• Substance Name: STRYCHNOS NUX-VOMICA SEED; HISTAMINE DIHYDROCHLORIDE; MANGANESE; SCHOENOCAULON OFFICINALE SEED; APIS MELLIFERA; SILVER NITRATE; ONION; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; SULFUR; ARSENIC TRIOXIDE
• Active Ingredient Strength: 4 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 17089-476-20

2 TUBE in 1 BOX (17089-476-20) > 4 g in 1 TUBE

• Marketing Start Date: 2021-02-17
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details