NDC 57955-6021

Gout Symptom Formula

Natural Medicine

Gout Symptom Formula is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by King Bio Inc.. The primary component is Ammonium Phosphate, Dibasic; Atropa Belladonna; Colchicum Autumnale Bulb; Formic Acid; Fraxinus Excelsior Leaf; Ledum Palustre Twig; Sodium Carbonate; Strychnos Nux-vomica Seed; Urtica Urens.

Product ID57955-6021_116793df-8ad4-421e-99f3-0f9483053ea5
NDC57955-6021
Product TypeHuman Otc Drug
Proprietary NameGout Symptom Formula
Generic NameNatural Medicine
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-11-18
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameKing Bio Inc.
Substance NameAMMONIUM PHOSPHATE, DIBASIC; ATROPA BELLADONNA; COLCHICUM AUTUMNALE BULB; FORMIC ACID; FRAXINUS EXCELSIOR LEAF; LEDUM PALUSTRE TWIG; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; URTICA URENS
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
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 57955-6021-2

59 mL in 1 BOTTLE, SPRAY (57955-6021-2)
Marketing Start Date2011-11-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57955-6021-2 [57955602102]

Gout Symptom Formula LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-11-18
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
AMMONIUM PHOSPHATE, DIBASIC10 [hp_X]/59mL

OpenFDA Data

SPL SET ID:2402fb8d-b73b-41b3-9475-7e5927cab665
Manufacturer
UNII

NDC Crossover Matching brand name "Gout Symptom Formula" or generic name "Natural Medicine"

NDCBrand NameGeneric Name
57955-2826Gout Symptom FormulaAmmonium phosphoricum, Belladonna, Colchicum autumnale, Formicum acidum, Fraxinus excelsior, Ledum palustre, Natrum carbonicum, Nux vomica, Urtica urens.
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