Ledum Combination 9257 (ledum combination) NDC 63083-9257

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-9257Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-9257Add 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
63083-9257-1	63083925701	29.5 mL in 1 BOTTLE, DROPPER (63083-9257-1)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): Ledum Combination 9257Suffix: 9257
Generic name (nonproprietary): ledum combination
Active ingredients: Pseudognaphalium obtusifolium whole — 3 [hp_X]/29.5mLBerberis vulgaris root bark — 4 [hp_X]/29.5mLBlack cohosh — 4 [hp_X]/29.5mLCinchona officinalis bark — 4 [hp_X]/29.5mLRhododendron tomentosum leafy twig — 4 [hp_X]/29.5mLRanunculus bulbosus whole — 4 [hp_X]/29.5mLHorse chestnut — 6 [hp_X]/29.5mLSodium borate — 6 [hp_X]/29.5mLCitrullus colocynthis fruit pulp — 6 [hp_X]/29.5mLCupric acetate — 6 [hp_X]/29.5mLPotassium carbonate — 6 [hp_X]/29.5mLPicric acid — 6 [hp_X]/29.5mLPulsatilla montana whole — 6 [hp_X]/29.5mLClaviceps purpurea sclerotium — 6 [hp_X]/29.5mLSilicon dioxide — 6 [hp_X]/29.5mLAmmonium cation — 8 [hp_X]/29.5mLBos taurus bone marrow — 8 [hp_X]/29.5mLBovine type ii collagen (Tracheal cartilage) — 8 [hp_X]/29.5mLBos taurus intervertebral disc — 8 [hp_X]/29.5mLSus scrofa adrenal gland — 10 [hp_X]/29.5mLSilver — 10 [hp_X]/29.5mLAnhydrous dibasic calcium phosphate — 10 [hp_X]/29.5mLMercuric oxide — 10 [hp_X]/29.5mLSepia officinalis juice — 10 [hp_X]/29.5mLZinc — 10 [hp_X]/29.5mLGonorrheal urethral secretion human — 12 [hp_X]/29.5mLSulfur — 30 [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 63083-9257_d444afc7-9686-4d89-888d-a9c48c9192bfSPL ID d444afc7-9686-4d89-888d-a9c48c9192bfSPL set ID 38b89b32-4915-487d-8b2d-250123487b15UNII 36XQ854NWW, 1TH8Q20J0U, K73E24S6X9, S003A158SB, 877L01IZ0P, AEQ8NXJ0MB, 3C18L6RJAZ, 91MBZ8H3QO, 23H32AOH17, 39M11XPH03, BQN1B9B9HA, A49OS0F91S, 24K790T39B, 01G9XEA93N, ETJ7Z6XBU4, 54S68520I4, 08X0K2M57P, 76TK29UQEZ, 0A04Z76C13, 398IYQ16YV, 3M4G523W1G, L11K75P92J, IY191986AO, QDL83WN8C2, J41CSQ7QDS, 9BZG9E3I8F, 70FD1KFU70

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

N463083925701 followed by a unit qualifier and the quantity

Package 63083-9257-01. 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 mild joint, muscle, or back pain, stiffness, or tenderness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)