NDC 35896-001

Super HG

Aralia Quinquefolia, Arnica Montana, Carduus Marianus, Damiana, Galium Aparine, Hamamelis Virginiana, Hepar Suis, Natrum Muriaticum, Phosphoricum Acidum, Pituitarum Posterium, Taraxacum Officinale, Thuja Occidentalis

Super HG is a Sublingual Liquid in the Human Otc Drug category. It is labeled and distributed by Physician's Choice, Inc.. The primary component is American Ginseng; Arnica Montana; Silybum Marianum Seed; Turnera Diffusa Leafy Twig; Galium Aparine; Hamamelis Virginiana Root Bark/stem Bark; Pork Liver; Sodium Chloride; Phosphoric Acid; Sus Scrofa Pituitary Gland; Taraxacum Officinale; Thuja Occidentalis Leafy Twig.

Product ID35896-001_904cff57-9047-4ed7-84c8-fadd4d0fff8b
NDC35896-001
Product TypeHuman Otc Drug
Proprietary NameSuper HG
Generic NameAralia Quinquefolia, Arnica Montana, Carduus Marianus, Damiana, Galium Aparine, Hamamelis Virginiana, Hepar Suis, Natrum Muriaticum, Phosphoricum Acidum, Pituitarum Posterium, Taraxacum Officinale, Thuja Occidentalis
Dosage FormLiquid
Route of AdministrationSUBLINGUAL
Marketing Start Date2013-05-15
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NamePhysician's Choice, Inc.
Substance NameAMERICAN GINSENG; ARNICA MONTANA; SILYBUM MARIANUM SEED; TURNERA DIFFUSA LEAFY TWIG; GALIUM APARINE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; PORK LIVER; SODIUM CHLORIDE; PHOSPHORIC ACID; SUS SCROFA PITUITARY GLAND; TARAXACUM OFFICINALE; THUJA OCCIDENTALIS LEAFY TWIG
Active Ingredient Strength3 [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_C]/30mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 35896-001-30

1 BOTTLE, SPRAY in 1 CARTON (35896-001-30) > 30 mL in 1 BOTTLE, SPRAY
Marketing Start Date2013-05-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 35896-001-30 [35896000130]

Super HG LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-05-15
Inactivation Date2019-11-27

Drug Details


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