NDC 49726-023

Goutinex Gout Symptom Relief

Actaea Spicata, Ammonium Phosphoricum, Belladonna, Colchicum Autumnale, Formicum Acidum, Fraxinus Excelsior, Ledum Palustre, Natrum Carbonicum, Nux Vomica, Phytolacca Decandra, Rhododendron Chrysanthum, Salicylicum Acidum, Urtica Urens

Goutinex Gout Symptom Relief is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Hello Life, Inc.. The primary component is Actaea Spicata Root; Ammonium Phosphate, Dibasic; Atropa Belladonna; Colchicum Autumnale Bulb; Formic Acid; Sodium Carbonate; Strychnos Nux-vomica Seed; Phytolacca Americana Root; Rhododendron Aureum Leaf; Salicylic Acid; Urtica Urens; Ledum Palustre Twig; Fraxinus Excelsior Leaf.

Product ID49726-023_7df183c1-5f62-1a16-e053-2991aa0a2223
NDC49726-023
Product TypeHuman Otc Drug
Proprietary NameGoutinex Gout Symptom Relief
Generic NameActaea Spicata, Ammonium Phosphoricum, Belladonna, Colchicum Autumnale, Formicum Acidum, Fraxinus Excelsior, Ledum Palustre, Natrum Carbonicum, Nux Vomica, Phytolacca Decandra, Rhododendron Chrysanthum, Salicylicum Acidum, Urtica Urens
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-11-09
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHello Life, Inc.
Substance NameACTAEA SPICATA ROOT; AMMONIUM PHOSPHATE, DIBASIC; ATROPA BELLADONNA; COLCHICUM AUTUMNALE BULB; FORMIC ACID; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; PHYTOLACCA AMERICANA ROOT; RHODODENDRON AUREUM LEAF; SALICYLIC ACID; URTICA URENS; LEDUM PALUSTRE TWIG; FRAXINUS EXCELSIOR LEAF
Active Ingredient Strength10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49726-023-02

1 BOTTLE, DROPPER in 1 CARTON (49726-023-02) > 59 mL in 1 BOTTLE, DROPPER
Marketing Start Date2011-11-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49726-023-02 [49726002302]

Goutinex Gout Symptom Relief LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-11-09
Inactivation Date2020-01-31

Drug Details


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