United States · FDA National Drug Code directory

Gout Drops 2080

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 63083-2080_de14e93f-43cf-4282-9aa8-58808df90c38
Product NDC: 63083-2080
Form: LIQUID
Composition / generic term: Gout Drops
Labeler: Professional Complementary Health Formulas
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 19840815
Source listing expiry: 20271231

Source-listed ingredients

BRYONIA ALBA ROOT — 4 [hp_X]/59mL
SOLANUM DULCAMARA WHOLE — 4 [hp_X]/59mL
RHODODENDRON TOMENTOSUM LEAFY TWIG — 4 [hp_X]/59mL
ARNICA MONTANA WHOLE — 6 [hp_X]/59mL
BENZOIC ACID — 6 [hp_X]/59mL
COLCHICUM AUTUMNALE BULB — 6 [hp_X]/59mL
LITHIUM CARBONATE — 6 [hp_X]/59mL
URTICA URENS WHOLE — 6 [hp_X]/59mL
FORMICA RUFA — 12 [hp_X]/59mL
LYCOPODIUM CLAVATUM SPORE — 12 [hp_X]/59mL

These values do not establish equivalence or a dose recommendation.

Packages

59 mL in 1 BOTTLE, DROPPER (63083-2080-2) · 63083-2080-2

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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