Cell Energy Performance Drops 2048 NDC 63083-2048

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2048Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2048Add 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
63083-2048-2	63083204802	59 mL in 1 BOTTLE, DROPPER (63083-2048-2)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): Cell Energy Performance Drops 2048Suffix: 2048
Generic name (nonproprietary): cell energy performance drops
Active ingredients: Vitis vinifera seed — 6 [hp_X]/59mLAnhydrous citric acid — 8 [hp_X]/59mLCoenzyme a — 8 [hp_X]/59mLNadh — 8 [hp_X]/59mLPhosphorus — 9 [hp_X]/59mLCalcium pyruvate — 12 [hp_X]/59mLGermanium — 12 [hp_X]/59mLAnhydrous dextrose — 12 [hp_X]/59mLCarnitine — 30 [hp_X]/59mLUbidecarenone — 30 [hp_X]/59mLIron — 30 [hp_X]/59mLLactic acid, Dl- — 30 [hp_X]/59mLRiboflavin — 30 [hp_X]/59mLAlpha lipoic acid — 30 [hp_X]/59mLAdenosine triphosphate — 30 [hp_X]/59mLCarbon dioxide — 200 [hp_X]/59mLDalotuzumab — 200 [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: Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)X-Ray Contrast Activity (Mechanism)
Identifiers: Product ID 63083-2048_52591072-1eb9-40c9-88cc-9a280eb9c56aSPL ID 52591072-1eb9-40c9-88cc-9a280eb9c56aSPL set ID 8701ea61-5d5f-466b-8d2c-f808e7b4d8feUNII C34U15ICXA, XF417D3PSL, SAA04E81UX, 4J24DQ0916, 27YLU75U4W, 9V2CQZ19N4, 00072J7XWS, 5SL0G7R0OK, S7UI8SM58A, EJ27X76M46, E1UOL152H7, 3B8D35Y7S4, TLM2976OFR, 73Y7P0K73Y, 8L70Q75FXE, 142M471B3J, 6YI1L648RH
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent; Radiographic Contrast Agent

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

N463083204802 followed by a unit qualifier and the quantity

Package 63083-2048-02. 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 exhaustion, muscle weakness, lethargy, or tiring easily.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)