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Gout Symptom Formula - 57955-6021-2 - (Natural Medicine)

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Drug Information of Gout Symptom Formula

Product NDC: 57955-6021
Proprietary Name: Gout Symptom Formula
Non Proprietary Name: Natural Medicine
Active Ingredient(s): 10; 10; 10; 10; 10; 10; 10; 10; 10    [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 & nbsp;   Natural Medicine
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Gout Symptom Formula

Product NDC: 57955-6021
Labeler Name: King Bio Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20111118

Package Information of Gout Symptom Formula

Package NDC: 57955-6021-2
Package Description: 59 mL in 1 BOTTLE, SPRAY (57955-6021-2)

NDC Information of Gout Symptom Formula

NDC Code 57955-6021-2
Proprietary Name Gout Symptom Formula
Package Description 59 mL in 1 BOTTLE, SPRAY (57955-6021-2)
Product NDC 57955-6021
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Natural Medicine
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20111118
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name King Bio Inc.
Substance Name AMMONIUM PHOSPHATE, DIBASIC; ATROPA BELLADONNA; COLCHICUM AUTUMNALE BULB; FORMIC ACID; FRAXINUS EXCELSIOR LEAF; LEDUM PALUSTRE TWIG; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; URTICA URENS
Strength Number 10; 10; 10; 10; 10; 10; 10; 10; 10
Strength Unit [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
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