United States · FDA National Drug Code directory

Tinnitus Drops 2072

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: 63083-2072_81eecf06-9f70-47e0-9b9c-3dd85170255a
Product NDC: 63083-2072
Form: LIQUID
Composition / generic term: Tinnitus Drops
Labeler: Professional Complementary Health Formulas
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 19840815
Source listing expiry: 20271231

Source-listed ingredients

BLACK COHOSH — 1 [hp_X]/59mL
GINKGO — 1 [hp_X]/59mL
CINCHONA OFFICINALIS BARK — 3 [hp_X]/59mL
GOLDENSEAL — 5 [hp_X]/59mL
SUS SCROFA EAR — 6 [hp_X]/59mL
LYCOPODIUM CLAVATUM SPORE — 6 [hp_X]/59mL
BOS TAURUS NERVE — 6 [hp_X]/59mL
SULFUR — 6 [hp_X]/59mL
DIGITALIS — 12 [hp_X]/59mL
POTASSIUM CARBONATE — 30 [hp_X]/59mL

These values do not establish equivalence or a dose recommendation.

Packages

59 mL in 1 BOTTLE, DROPPER (63083-2072-2) · 63083-2072-2

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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