Multi-Potency Growth Hormone Drops 2162 NDC 63083-2162

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2162Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2162Add 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
63083-2162-2	63083216202	59 mL in 1 BOTTLE, DROPPER (63083-2162-2)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): Multi-Potency Growth Hormone Drops 2162Suffix: 2162
Generic name (nonproprietary): multi-potency growth hormone drops
Active ingredients: Somatropin — 6 [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: Human Growth Hormone (Chemical structure)
Identifiers: Product ID 63083-2162_94769185-8a02-4c77-83dd-71bb14a2c3e2SPL ID 94769185-8a02-4c77-83dd-71bb14a2c3e2SPL set ID 290c3250-b6cd-499f-902c-ebdbfb2dc4e3UNII NQX9KB6PCL
Pharmacologic class: Recombinant Human Growth Hormone

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

N463083216202 followed by a unit qualifier and the quantity

Package 63083-2162-02. 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 feeling tired, listless, easily fatigued, or experiencing reduced strength, difficulty concentrating, or a lack of motivation.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)