DNA Insulin Drops 2019 (dna insulin drops) NDC 63083-2019

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2019Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2019Add 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
63083-2019-2	63083201902	59 mL in 1 BOTTLE, DROPPER (63083-2019-2)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): DNA Insulin Drops 2019Suffix: 2019
Generic name (nonproprietary): dna insulin drops
Active ingredients: Chromium — 6 [hp_X]/59mLLycopodium clavatum spore — 6 [hp_X]/59mLVanadium — 6 [hp_X]/59mLPancrelipase amylase — 6 [hp_X]/59mLInsulin glulisine — 12 [hp_X]/59mLPhosphoric acid — 30 [hp_X]/59mLUranyl nitrate hexahydrate — 30 [hp_X]/59mLRadium bromide — 60 [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)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Insulin (Chemical/Ingredient)
Identifiers: Product ID 63083-2019_91ade3ff-25ab-464b-8084-9fb5d5d6d955SPL ID 91ade3ff-25ab-464b-8084-9fb5d5d6d955SPL set ID 527dbb62-5c68-4ea8-93c7-48122817d6a5UNII 0R0008Q3JB, C88X29Y479, 00J9J9XKDE, YOJ58O116E, 7XIY785AZD, E4GA8884NN, 3V057702FY, R74O7T8569
Pharmacologic class: Insulin Analog; 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

N463083201902 followed by a unit qualifier and the quantity

Package 63083-2019-02. 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 increased hunger or thirst, frequent urination, fatigue, nausea, or vomiting.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)