Hypothalamus/Adrenal/Pituitary Drops 5032 NDC 63083-5032

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-5032Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-5032Add 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
63083-5032-2	63083503202	59 mL in 1 BOTTLE, DROPPER (63083-5032-2)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): Hypothalamus/Adrenal/Pituitary Drops 5032Suffix: 5032
Generic name (nonproprietary): hypothalamus/adrenal/pituitary drops
Active ingredients: Berberis vulgaris root bark — 3 [hp_X]/59mLPhosphorus — 6 [hp_X]/59mLCinchona officinalis bark — 8 [hp_X]/59mLSus scrofa adrenal gland — 8 [hp_X]/59mLBos taurus hypothalamus — 8 [hp_X]/59mLBos taurus pituitary gland, Posterior — 8 [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 63083-5032_25eb5497-91d3-4abf-8398-da5e7b0bbea6SPL ID 25eb5497-91d3-4abf-8398-da5e7b0bbea6SPL set ID f795b0b0-d4f9-447a-9d94-33daa3eef8e8UNII 1TH8Q20J0U, 27YLU75U4W, S003A158SB, 398IYQ16YV, S6G2NLH4Y7, 7JM57I419K

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

N463083503202 followed by a unit qualifier and the quantity

Package 63083-5032-02. 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 stress, fatigue, disturbed sleep, or brain fog.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)