Sepia Combination 9246 (sepia combination) NDC 63083-9246

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-9246Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-9246Add 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
63083-9246-1	63083924601	29.5 mL in 1 BOTTLE, DROPPER (63083-9246-1)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): Sepia Combination 9246Suffix: 9246
Generic name (nonproprietary): sepia combination
Active ingredients: Potassium bromide — 4 [hp_X]/29.5mLStrychnos ignatii seed — 4 [hp_X]/29.5mLPhosphoric acid — 4 [hp_X]/29.5mLSepia officinalis juice — 4 [hp_X]/29.5mLZinc valerate dihydrate — 8 [hp_X]/29.5mLScabies lesion lysate (Human) — 12 [hp_X]/29.5mL
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 63083-9246_06b7e030-310d-4195-90ad-6d7ed17e2adbSPL ID 06b7e030-310d-4195-90ad-6d7ed17e2adbSPL set ID fe79986b-7b2d-4cfd-8386-45de02115ca9UNII OSD78555ZM, 1NM3M2487K, E4GA8884NN, QDL83WN8C2, MN0RX54EQA, 5UAU16Z1U4

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

N463083924601 followed by a unit qualifier and the quantity

Package 63083-9246-01. 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 mental fatigue or exhaustion, anxiousness, or insomnia.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)