NDC 17089-306

GUNA-DIZZY

.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 -

GUNA-DIZZY is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Epinephrine; .alpha.-ketoglutaric Acid; Ambergris; Sus Scrofa Artery; Sus Scrofa Cerebellum; Quinine Salicylate; Anamirta Cocculus Seed; Conium Maculatum Flowering Top; Fumaric Acid; Malic Acid; Melatonin; Mineral Oil; Sus Scrofa Placenta; Pteridium Aquilinum Root; Pyridoxine Hydrochloride; Quinhydrone; Tobacco Leaf; Thiamine Hydrochloride.

Product ID17089-306_7e7be278-8d19-71c4-e053-2991aa0a377c
NDC17089-306
Product TypeHuman Otc Drug
Proprietary NameGUNA-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 -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2006-05-23
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameEPINEPHRINE; .ALPHA.-KETOGLUTARIC ACID; AMBERGRIS; SUS SCROFA ARTERY; SUS SCROFA CEREBELLUM; QUININE SALICYLATE; ANAMIRTA COCCULUS SEED; CONIUM MACULATUM FLOWERING TOP; FUMARIC ACID; MALIC ACID; MELATONIN; MINERAL OIL; SUS SCROFA PLACENTA; PTERIDIUM AQUILINUM ROOT; PYRIDOXINE HYDROCHLORIDE; QUINHYDRONE; TOBACCO LEAF; THIAMINE HYDROCHLORIDE
Active Ingredient Strength6 [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; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 17089-306-18

1 BOTTLE, DROPPER in 1 BOX (17089-306-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2018-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-306-18 [17089030618]

GUNA-DIZZY SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-21

Drug Details


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