Dementia Drops 2117 (dementia drops) NDC 63083-2117

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2117Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2117Add 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
63083-2117-2	63083211702	59 mL in 1 BOTTLE, DROPPER (63083-2117-2)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): Dementia Drops 2117Suffix: 2117
Generic name (nonproprietary): dementia drops
Active ingredients: Turnera diffusa leaf — 1 [hp_X]/59mLCelery seed — 3 [hp_X]/59mLAnhydrous dibasic calcium phosphate — 3 [hp_X]/59mLHyoscyamus niger — 4 [hp_X]/59mLBarium carbonate — 6 [hp_X]/59mLOyster shell calcium carbonate, Crude — 6 [hp_X]/59mLPhosphoric acid — 6 [hp_X]/59mLZinc — 6 [hp_X]/59mLGold monoiodide — 8 [hp_X]/59mLPicric acid — 10 [hp_X]/59mLPhosphorus — 12 [hp_X]/59mLLilium lancifolium whole flowering — 12 [hp_X]/59mLSulfur — 30 [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
Identifiers: Product ID 63083-2117_fa0c95e9-b87d-4699-9ee4-168e1981c55aSPL ID fa0c95e9-b87d-4699-9ee4-168e1981c55aSPL set ID 83aec02b-bc62-49a2-ba35-4ac94f9bfc6eUNII 812R0W1I3K, 1G1EAA320L, L11K75P92J, 4WRK2153H3, 6P669D8HQ8, 2E32821G6I, E4GA8884NN, J41CSQ7QDS, T1UDV7ES1A, A49OS0F91S, 27YLU75U4W, X67Z2963PI, 70FD1KFU70

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

N463083211702 followed by a unit qualifier and the quantity

Package 63083-2117-02. 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 irritability, anxiousness, mood swings, forgetfulness, or confusion.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)