NDC 17089-461 – Guna Allergy

Histamine Dihydrochloride 200 [hp_X]/30mL; Sus Scrofa Adrenal Gland 6 [hp_X]/30mL; Epinephrine 6 [hp_X]/30mL; Apis Mellifera 200 [hp_X]/30mL; Cupric Acetate 12… · Solution/ Drops · Oral

Human Otc Drug

Product NDC17089-461

Product details

Brand name
Guna Allergy
Generic name
Adrenalinum - allium cepa - ammonium carbonicum - apis mellifica - argentum nitricum - arsenicum album - cuprum aceticum - galphimia glauca - glandula suprarenalis suis - histaminum hydrochloricum - luffa operculata - matricaria chamomilla - mucosa nasalis suis - natrum muriaticum - sabadilla - scilla maritima -
Labeler
Guna spa
Dosage form
Solution/ Drops
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 24, 2020
Listing expires
December 31, 2026
Pharmacologic class
Catecholamine; Non-Standardized Food Allergenic Extract; Standardized Insect Venom Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Guna Allergy →

Package NDC codes (1)

Package NDCDescriptionSince
17089-461-181 BOTTLE, DROPPER in 1 BOX (17089-461-18) / 30 mL in 1 BOTTLE, DROPPERSep 24, 2020