NDC 17089-350

GUNA-AWARENESS

Betaine - Bufo Bufo Cutaneous Gland - Calcium Carbonate - Chromic Sulfate - Cicuta Virosa Root - Copper - Folic Acid - Gold - Cobalamin - Iron - Lachesis Muta Venom - Melatonin - Molybdenum - Neurotrophin-3 - Neurotrophin-4 - Oxytocin - Silicon Dioxide - Sus Scrofa Frontal Lobe - Sus Scrofa Temporal Lobe - Thyrotropin Alfa - Ubidecarenone - Vanadium - Zinc - Brain-derived Neurotrophic Factor Human -

GUNA-AWARENESS is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Gold; Brain-derived Neurotrophic Factor Human; Bufo Bufo Cutaneous Gland; Calcium Carbonate; Chromic Sulfate; Cicuta Virosa Root; Cobalamin; Ubidecarenone; Copper; Iron; Folic Acid; Sus Scrofa Frontal Lobe; Lachesis Muta Venom; Melatonin; Molybdenum; Neurotrophin-3; Neurotrophin-4; Oxytocin; Silicon Dioxide; Sus Scrofa Temporal Lobe; Thyrotropin Alfa; Betaine; Vanadium; Zinc.

Product ID17089-350_7d9b872d-b3aa-64a9-e053-2991aa0a7808
NDC17089-350
Product TypeHuman Otc Drug
Proprietary NameGUNA-AWARENESS
Generic NameBetaine - Bufo Bufo Cutaneous Gland - Calcium Carbonate - Chromic Sulfate - Cicuta Virosa Root - Copper - Folic Acid - Gold - Cobalamin - Iron - Lachesis Muta Venom - Melatonin - Molybdenum - Neurotrophin-3 - Neurotrophin-4 - Oxytocin - Silicon Dioxide - Sus Scrofa Frontal Lobe - Sus Scrofa Temporal Lobe - Thyrotropin Alfa - Ubidecarenone - Vanadium - Zinc - Brain-derived Neurotrophic Factor Human -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2008-04-16
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameGOLD; BRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN; BUFO BUFO CUTANEOUS GLAND; CALCIUM CARBONATE; CHROMIC SULFATE; CICUTA VIROSA ROOT; COBALAMIN; UBIDECARENONE; COPPER; IRON; FOLIC ACID; SUS SCROFA FRONTAL LOBE; LACHESIS MUTA VENOM; MELATONIN; MOLYBDENUM; NEUROTROPHIN-3; NEUROTROPHIN-4; OXYTOCIN; SILICON DIOXIDE; SUS SCROFA TEMPORAL LOBE; THYROTROPIN ALFA; BETAINE; VANADIUM; ZINC
Active Ingredient Strength12 [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; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/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 Through2019-12-31

Packaging

NDC 17089-350-18

1 BOTTLE, DROPPER in 1 BOX (17089-350-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2018-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-350-18 [17089035018]

GUNA-AWARENESS SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-21
Inactivation Date2020-01-31
Reactivation Date2020-03-13

Drug Details


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