Alopecia Formula 2139 (alopecia formula) NDC 63083-2139

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2139Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2139Add 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
63083-2139-2	63083213902	59 mL in 1 BOTTLE, DROPPER (63083-2139-2)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): Alopecia Formula 2139Suffix: 2139
Generic name (nonproprietary): alopecia formula
Active ingredients: Phosphorus — 6 [hp_X]/59mLSulfur — 6 [hp_X]/59mLDaphne mezereum bark — 9 [hp_X]/59mLSepia officinalis juice — 9 [hp_X]/59mLAluminum oxide — 12 [hp_X]/59mLLycopodium clavatum spore — 12 [hp_X]/59mLEclipta prostrata whole — 12 [hp_X]/59mLGraphite — 12 [hp_X]/59mLThallium — 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 63083-2139_f8335d21-022c-46e2-ae8b-79b2fc9c3502SPL ID f8335d21-022c-46e2-ae8b-79b2fc9c3502SPL set ID ce0eaf67-a435-4167-b9ce-c0ff1f8a9dc2UNII 27YLU75U4W, 70FD1KFU70, X2N6E405GV, QDL83WN8C2, LMI26O6933, C88X29Y479, 8138AB7E8Y, 4QQN74LH4O, AD84R52XLF

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

N463083213902 followed by a unit qualifier and the quantity

Package 63083-2139-02. 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 Temporarily relieves the effects of unexplained hair loss.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)