tinnitus drops 2072

Generic: tinnitus drops

Labeler: professional complementary health formulas
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name tinnitus drops 2072
Generic Name tinnitus drops
Labeler professional complementary health formulas
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

black cohosh 1 [hp_X]/59mL, bos taurus nerve 6 [hp_X]/59mL, cinchona officinalis bark 3 [hp_X]/59mL, digitalis 12 [hp_X]/59mL, ginkgo 1 [hp_X]/59mL, goldenseal 5 [hp_X]/59mL, lycopodium clavatum spore 6 [hp_X]/59mL, potassium carbonate 30 [hp_X]/59mL, sulfur 6 [hp_X]/59mL, sus scrofa ear 6 [hp_X]/59mL

Manufacturer
Professional Complementary Health Formulas

Identifiers & Regulatory

Product NDC 63083-2072
Product ID 63083-2072_81eecf06-9f70-47e0-9b9c-3dd85170255a
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2027-12-31
Marketing Start 1984-08-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 630832072
Hyphenated Format 63083-2072

Supplemental Identifiers

UNII
K73E24S6X9 28G2U3MQJK S003A158SB F1T8QT9U8B 19FUJ2C58T ZW3Z11D0JV C88X29Y479 BQN1B9B9HA 70FD1KFU70 7DX2J287CV

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name tinnitus drops 2072 (source: ndc)
Generic Name tinnitus drops (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 [hp_X]/59mL
  • 6 [hp_X]/59mL
  • 3 [hp_X]/59mL
  • 12 [hp_X]/59mL
  • 5 [hp_X]/59mL
  • 30 [hp_X]/59mL
source: ndc
Packaging
  • 59 mL in 1 BOTTLE, DROPPER (63083-2072-2)
source: ndc

Packages (1)

Ingredients (10)

black cohosh (1 [hp_X]/59mL) bos taurus nerve (6 [hp_X]/59mL) cinchona officinalis bark (3 [hp_X]/59mL) digitalis (12 [hp_X]/59mL) ginkgo (1 [hp_X]/59mL) goldenseal (5 [hp_X]/59mL) lycopodium clavatum spore (6 [hp_X]/59mL) potassium carbonate (30 [hp_X]/59mL) sulfur (6 [hp_X]/59mL) sus scrofa ear (6 [hp_X]/59mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "81eecf06-9f70-47e0-9b9c-3dd85170255a", "openfda": {"unii": ["K73E24S6X9", "28G2U3MQJK", "S003A158SB", "F1T8QT9U8B", "19FUJ2C58T", "ZW3Z11D0JV", "C88X29Y479", "BQN1B9B9HA", "70FD1KFU70", "7DX2J287CV"], "spl_set_id": ["24649b5b-ed21-4a32-8501-196b9e1348bb"], "manufacturer_name": ["Professional Complementary Health Formulas"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, DROPPER (63083-2072-2)", "package_ndc": "63083-2072-2", "marketing_start_date": "19850815"}], "brand_name": "Tinnitus Drops 2072", "product_id": "63083-2072_81eecf06-9f70-47e0-9b9c-3dd85170255a", "dosage_form": "LIQUID", "product_ndc": "63083-2072", "generic_name": "Tinnitus Drops", "labeler_name": "Professional Complementary Health Formulas", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tinnitus Drops", "brand_name_suffix": "2072", "active_ingredients": [{"name": "BLACK COHOSH", "strength": "1 [hp_X]/59mL"}, {"name": "BOS TAURUS NERVE", "strength": "6 [hp_X]/59mL"}, {"name": "CINCHONA OFFICINALIS BARK", "strength": "3 [hp_X]/59mL"}, {"name": "DIGITALIS", "strength": "12 [hp_X]/59mL"}, {"name": "GINKGO", "strength": "1 [hp_X]/59mL"}, {"name": "GOLDENSEAL", "strength": "5 [hp_X]/59mL"}, {"name": "LYCOPODIUM CLAVATUM SPORE", "strength": "6 [hp_X]/59mL"}, {"name": "POTASSIUM CARBONATE", "strength": "30 [hp_X]/59mL"}, {"name": "SULFUR", "strength": "6 [hp_X]/59mL"}, {"name": "SUS SCROFA EAR", "strength": "6 [hp_X]/59mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19840815", "listing_expiration_date": "20271231"}