What is NDC 63083-2072?

63083-2072 is the product NDC for Tinnitus Drops 2072 (tinnitus drops), Black cohosh 1 [hp_X]/59mL + 9 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Tinnitus Drops 2072 (Tinnitus Drops).

What is the active ingredient?

Black cohosh, Ginkgo, Cinchona officinalis bark, Goldenseal, Sus scrofa ear, Lycopodium clavatum spore, Bos taurus nerve, Sulfur, Digitalis, Potassium carbonate.

Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Tinnitus Drops 2072?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Tinnitus Drops 2072 NDC 63083-2072

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2072Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2072Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
63083-2072-2	6308320720263083207202	59 mL in 1 BOTTLE, DROPPER (63083-2072-2)Marketed from Aug 15, 1985

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Tinnitus Drops 2072Suffix: 2072
Generic name (nonproprietary): tinnitus drops
Active ingredients: Black cohosh — 1 [hp_X]/59mLGinkgo — 1 [hp_X]/59mLCinchona officinalis bark — 3 [hp_X]/59mLGoldenseal — 5 [hp_X]/59mLSus scrofa ear — 6 [hp_X]/59mLLycopodium clavatum spore — 6 [hp_X]/59mLBos taurus nerve — 6 [hp_X]/59mLSulfur — 6 [hp_X]/59mLDigitalis — 12 [hp_X]/59mLPotassium carbonate — 30 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health FormulasNDC labeler code 63083
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Identifiers: Product ID 63083-2072_81eecf06-9f70-47e0-9b9c-3dd85170255aSPL ID 81eecf06-9f70-47e0-9b9c-3dd85170255aSPL set ID 24649b5b-ed21-4a32-8501-196b9e1348bbUNII K73E24S6X9, 19FUJ2C58T, S003A158SB, ZW3Z11D0JV, 7DX2J287CV, C88X29Y479, 28G2U3MQJK, 70FD1KFU70, F1T8QT9U8B, BQN1B9B9HA

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463083207202 followed by a unit qualifier and the quantity

Package 63083-2072-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 8, 2026.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-2072

What is NDC 63083-2072?: 63083-2072 is the product NDC for Tinnitus Drops 2072 (tinnitus drops), Black cohosh 1 [hp_X]/59mL + 9 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Tinnitus Drops 2072 (Tinnitus Drops).
What is the active ingredient?: Black cohosh, Ginkgo, Cinchona officinalis bark, Goldenseal, Sus scrofa ear, Lycopodium clavatum spore, Bos taurus nerve, Sulfur, Digitalis, Potassium carbonate.
Who is the labeler?: Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Tinnitus Drops 2072?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Tinnitus Drops 2072 (Tinnitus drops) NDC 63083-2072