What is NDC 63083-2089?

63083-2089 is the product NDC for Pain Formula I Drops 2089 (pain formula i drops), Coffea arabica seed, Roasted 3 [hp_X]/59mL + 5 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?

Pain Formula I Drops 2089 (Pain Formula I Drops).

What is the active ingredient?

Coffea arabica seed, Roasted, Amaryllis belladonna whole, Aconitum napellus whole, Bryonia alba root, Spigelia marilandica root, Magnesium phosphate, Dibasic trihydrate.

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 Pain Formula I Drops 2089?

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.

Pain Formula I Drops 2089 NDC 63083-2089

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2089Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2089Add 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
63083-2089-2	6308320890263083208902	59 mL in 1 BOTTLE, DROPPER (63083-2089-2)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): Pain Formula I Drops 2089Suffix: 2089
Generic name (nonproprietary): pain formula i drops
Active ingredients: Coffea arabica seed, Roasted — 3 [hp_X]/59mLAmaryllis belladonna whole — 4 [hp_X]/59mLAconitum napellus whole — 5 [hp_X]/59mLBryonia alba root — 5 [hp_X]/59mLSpigelia marilandica root — 6 [hp_X]/59mLMagnesium phosphate, Dibasic trihydrate — 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: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 63083-2089_8328d66f-3b47-428d-8601-d15b233dd337SPL ID 8328d66f-3b47-428d-8601-d15b233dd337SPL set ID fe6aeed7-95de-4ca0-828e-61451b467c72UNII 9H58JRT35E, 11B89M58UN, U0NQ8555JD, T7J046YI2B, 467D26HS0B, HF539G9L3Q
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N463083208902 followed by a unit qualifier and the quantity

Package 63083-2089-02. 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 minor aches or pain, particularly when improved by touch, massage, or pressure.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-2089

What is NDC 63083-2089?: 63083-2089 is the product NDC for Pain Formula I Drops 2089 (pain formula i drops), Coffea arabica seed, Roasted 3 [hp_X]/59mL + 5 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?: Pain Formula I Drops 2089 (Pain Formula I Drops).
What is the active ingredient?: Coffea arabica seed, Roasted, Amaryllis belladonna whole, Aconitum napellus whole, Bryonia alba root, Spigelia marilandica root, Magnesium phosphate, Dibasic trihydrate.
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 Pain Formula I Drops 2089?: 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.

Pain Formula I Drops 2089 (Pain formula i drops) NDC 63083-2089