Pineal/Pituitary/Hypothalamus Drops 5022 NDC 63083-5022

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-5022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-5022Add 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
63083-5022-2	63083502202	59 mL in 1 BOTTLE, DROPPER (63083-5022-2)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): Pineal/Pituitary/Hypothalamus Drops 5022Suffix: 5022
Generic name (nonproprietary): pineal/pituitary/hypothalamus drops
Active ingredients: Chaste tree fruit — 3 [hp_X]/59mLBos taurus hypothalamus — 6 [hp_X]/59mLSus scrofa pineal gland — 6 [hp_X]/59mLBos taurus pituitary gland, Posterior — 6 [hp_X]/59mLStrychnos ignatii seed — 12 [hp_X]/59mLPhosphoric acid — 12 [hp_X]/59mLPicric acid — 12 [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 63083-5022_30584e26-7d77-4bd8-9094-96a8136f9e0dSPL ID 30584e26-7d77-4bd8-9094-96a8136f9e0dSPL set ID 97307e9b-5da3-40d3-a619-0722ca306980UNII 433OSF3U8A, S6G2NLH4Y7, 050QZ2EDK7, 7JM57I419K, 1NM3M2487K, E4GA8884NN, A49OS0F91S

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

N463083502202 followed by a unit qualifier and the quantity

Package 63083-5022-02. 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 fatigue, weakness, sadness, sleep disturbance, minor muscle aches, occasional headache, dizziness, mood changes or swings, dry skin, weight gain, or constipation.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)