What is NDC 83027-0006?

83027-0006 is the product NDC for Tinnitus Formula, Black cohosh 2 [hp_X]/mL + 9 more ingredients spray, listed with the FDA by Nutritional Specialties, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Tinnitus Formula (Cimicifuga Racemosa, Ginkgo Biloba, Cinchona Officinalis, Hydrastis Canadensis, Lycopodium Clavatum, Sulphur, Cerebellum (Suis), Ear (Suis) Digitalis Purpurea, Kali Carbonicum).

What is the active ingredient?

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

Nutritional Specialties, Inc., NDC labeler code 83027. 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 Formula?

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 Formula NDC 83027-0006 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)83027-0006Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83027-0006Add 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
83027-0006-1	8302700060183027000601	60 mL in 1 BOTTLE, SPRAY (83027-0006-1)Marketed from Apr 10, 2023

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 Formula
Generic name (nonproprietary): cimicifuga racemosa, ginkgo biloba, cinchona officinalis, hydrastis canadensis, lycopodium clavatum, sulphur, cerebellum (suis), ear (suis) digitalis purpurea, kali carbonicum
Active ingredients: Black cohosh — 2 [hp_X]/mLGinkgo — 2 [hp_X]/mLCinchona officinalis bark — 3 [hp_X]/mLGoldenseal — 6 [hp_X]/mLLycopodium clavatum spore — 6 [hp_X]/mLSulfur — 6 [hp_X]/mLSus scrofa cerebrum — 6 [hp_X]/mLSus scrofa ear — 6 [hp_X]/mLDigitalis — 12 [hp_X]/mLPotassium carbonate — 30 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Nutritional Specialties, Inc.NDC labeler code 83027
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 10, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 83027-0006_b6fde97d-9326-4d8f-ade3-40658649fd73SPL ID b6fde97d-9326-4d8f-ade3-40658649fd73SPL set ID 4885c23c-093c-4ea0-8061-83cdeab9902eUNII K73E24S6X9, 19FUJ2C58T, S003A158SB, ZW3Z11D0JV, C88X29Y479, 70FD1KFU70, 4GB5DQR532, 7DX2J287CV, F1T8QT9U8B, BQN1B9B9HAUPC 0649818032140

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

N483027000601 followed by a unit qualifier and the quantity

Package 83027-0006-01. 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 Oct 6, 2025.

Indications (excerpt from the label)

USES: Provides homeopathic assistance in relieving symptoms associated with tinnitus such as ringing in the ears, noises, and dizziness.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 83027-0006

What is NDC 83027-0006?: 83027-0006 is the product NDC for Tinnitus Formula, Black cohosh 2 [hp_X]/mL + 9 more ingredients spray, listed with the FDA by Nutritional Specialties, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Tinnitus Formula (Cimicifuga Racemosa, Ginkgo Biloba, Cinchona Officinalis, Hydrastis Canadensis, Lycopodium Clavatum, Sulphur, Cerebellum (Suis), Ear (Suis) Digitalis Purpurea, Kali Carbonicum).
What is the active ingredient?: Black cohosh, Ginkgo, Cinchona officinalis bark, Goldenseal, Lycopodium clavatum spore, Sulfur, Sus scrofa cerebrum, Sus scrofa ear, Digitalis, Potassium carbonate.
Who is the labeler?: Nutritional Specialties, Inc., NDC labeler code 83027. 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 Formula?: 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.