Pancreas Drops 5020 (pancreas drops) NDC 63083-5020

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-5020Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-5020Add 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
63083-5020-2	63083502002	59 mL in 1 BOTTLE, DROPPER (63083-5020-2)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): Pancreas Drops 5020Suffix: 5020
Generic name (nonproprietary): pancreas drops
Active ingredients: Artemisia annua flowering top — 3 [hp_X]/59mLFoeniculum vulgare fruit — 3 [hp_X]/59mLGlycyrrhiza glabra — 3 [hp_X]/59mLAchillea millefolium whole — 3 [hp_X]/59mLSyzygium cumini seed — 3 [hp_X]/59mLBilberry — 3 [hp_X]/59mLAcetic acid — 4 [hp_X]/59mLMarsdenia cundurango whole — 4 [hp_X]/59mLKidney bean — 4 [hp_X]/59mLSmilax ornata root — 4 [hp_X]/59mLGentiana lutea root — 6 [hp_X]/59mLBos taurus pancreas — 6 [hp_X]/59mLPancrelipase amylase — 6 [hp_X]/59mLUrea — 7 [hp_X]/59mLUric acid — 7 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
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)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 63083-5020_e12112f7-00a5-49eb-9813-2ee3df38df29SPL ID e12112f7-00a5-49eb-9813-2ee3df38df29SPL set ID 669a47a1-ae68-4b49-9f21-288314e9eb76UNII 0UQK6O82OW, J5W36Y5WG8, 2788Z9758H, 2FXJ6SW4PK, 820LSF646I, 9P2U39H18W, Q40Q9N063P, AT33ZFZ5A1, M98C8416QO, 2H1576D5WG, S72O3284MS, 1M529TNT1D, YOJ58O116E, 8W8T17847W, 268B43MJ25
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N463083502002 followed by a unit qualifier and the quantity

Package 63083-5020-02. 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 mild abdominal or back pain, bloating, nausea or vomiting, diarrhea, loss of appetite, or feelings of discomfort or uneasiness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)