What is NDC 63083-2120?

63083-2120 is the product NDC for Teething Drops 2120 (teething drops), Eugenol 3 [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?

Teething Drops 2120 (Teething Drops).

What is the active ingredient?

Eugenol, Ulmus rubra bark, Artemisia annua flowering top, Mentha x piperita whole, Clematis recta flowering top, Citrullus colocynthis fruit pulp, Copper, Myrrh, Bryonia alba root, Oyster shell calcium carbonate, Crude.

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 Teething Drops 2120?

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.

Teething Drops 2120 NDC 63083-2120 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2120Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2120Add 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
63083-2120-2	63083212002	59 mL in 1 BOTTLE, DROPPER (63083-2120-2)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): Teething Drops 2120Suffix: 2120
Generic name (nonproprietary): teething drops
Active ingredients: Eugenol — 3 [hp_X]/59mLUlmus rubra bark — 3 [hp_X]/59mLArtemisia annua flowering top — 3 [hp_X]/59mLMentha x piperita whole — 4 [hp_X]/59mLClematis recta flowering top — 6 [hp_X]/59mLCitrullus colocynthis fruit pulp — 6 [hp_X]/59mLCopper — 6 [hp_X]/59mLMyrrh — 6 [hp_X]/59mLBryonia alba root — 12 [hp_X]/59mLOyster shell calcium carbonate, Crude — 12 [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
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Histamine Release (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 63083-2120_f97c3e15-b5fe-476d-9cb4-4d565dd902d0SPL ID f97c3e15-b5fe-476d-9cb4-4d565dd902d0SPL set ID 31644007-d0a9-4482-a6b4-555b70686a72UNII 3T8H1794QW, 91QY4PXU8Q, 0UQK6O82OW, 79M2M2UDA9, 396421SP9F, 23H32AOH17, 789U1901C5, JC71GJ1F3L, T7J046YI2B, 2E32821G6I
Pharmacologic class: Copper-containing Intrauterine Device; Standardized Chemical Allergen

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

N463083212002 followed by a unit qualifier and the quantity

Package 63083-2120-02. 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 temporary relief of pain or irritability associated with teething.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-2120

What is NDC 63083-2120?: 63083-2120 is the product NDC for Teething Drops 2120 (teething drops), Eugenol 3 [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?: Teething Drops 2120 (Teething Drops).
What is the active ingredient?: Eugenol, Ulmus rubra bark, Artemisia annua flowering top, Mentha x piperita whole, Clematis recta flowering top, Citrullus colocynthis fruit pulp, Copper, Myrrh, Bryonia alba root, Oyster shell calcium carbonate, Crude.
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 Teething Drops 2120?: 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.

Teething Drops 2120 (Teething drops) NDC 63083-2120