Tinnitus Drops

FDA Drug Profile — Tinnitus Drops 2072

Tinnitus Drops is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Tinnitus Drops 2072. Available dosage form: liquid.

Drug Details

Generic Name
Tinnitus Drops
Brand Names
Tinnitus Drops 2072
Application Number
Sponsor
Professional Complementary Health Formulas
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
BLACK COHOSH, GINKGO, CINCHONA OFFICINALIS BARK, GOLDENSEAL, SUS SCROFA EAR, LYCOPODIUM CLAVATUM SPORE, BOS TAURUS NERVE, SULFUR, DIGITALIS, POTASSIUM CARBONATE

Indications and Usage

INDICATIONS For the temporary relief of noise in the ears, such as ringing, roaring, buzzing, hissing, or whistling.*

Warnings

WARNINGS Persistent symptoms may be a sign of a serious condition. If symptoms persist or are accompanied by a fever, persistent headache, dizziness, or loss of hearing, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.