GUNA-DIZZY

Product NDC

17089-306

11-digit product format

170890306

Labeler code

17089

Product ID

17089-306_7e7be278-8d19-71c4-e053-2991aa0a377c

Type

HUMAN OTC DRUG

Nonproprietary 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 -

Dosage form

SOLUTION/ DROPS

Route

ORAL

Labeler

Guna spa

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2006-05-23

Substance

.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 SALICYLATE; SUS SCROFA ARTERY; SUS SCROFA CEREBELLUM; SUS SCROFA PLACENTA; THIAMINE HYDROCHLORIDE; TOBACCO LEAF

Active strength

6; 6; 4; 3; 6; 6; 6; 4; 8; 8; 6; 6; 6; 6; 6; 6; 4; 6 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL

Pharmacologic classes

Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Analogs/Derivatives [Chemical/Ingredient], Antimalarial [EPC], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Depigmenting Activity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Melanin Synthesis Inhibitor [EPC], Melanin Synthesis Inhibitors [MoA], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes