NDC 17089-306 – Guna-dizzy

Epinephrine 6 [hp_X]/30mL; .alpha.-ketoglutaric Acid 6 [hp_X]/30mL; Ambergris 6 [hp_X]/30mL; Sus Scrofa Artery 6 [hp_X]/30mL; Sus Scrofa Cerebellum 6… · Solution/ Drops · Oral

Human Otc Drug

Product NDC17089-306

Product details

Brand name
Guna-dizzy
Generic name
.alpha.-ketoglutaric acid - ambergris - anamirta cocculus seed - conium maculatum flowering top - epinephrine - fumaric acid - malic acid - melatonin - mineral oil - pteridium aquilinum root - pyridoxine hydrochloride - quinhydrone - quinine - sus scrofa artery - sus scrofa cerebellum - sus scrofa placenta - thiamine hydrochloride - tobacco leaf -
Labeler
Guna spa
Dosage form
Solution/ Drops
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
May 23, 2006
Listing expires
December 31, 2026
Pharmacologic class
Antimalarial; Catecholamine; Melanin Synthesis Inhibitor; Non-Standardized Plant Allergenic Extract; Vitamin B6 Analog; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Guna-dizzy →

Package NDC codes (1)

Package NDCDescriptionSince
17089-306-181 BOTTLE, DROPPER in 1 BOX (17089-306-18) / 30 mL in 1 BOTTLE, DROPPERDec 21, 2018