What is NDC 48951-4203?

48951-4203 is the product NDC for Formica Oxalis, Oxalis acetosella leaf 3 [hp_X]/mL; Formica rufa 5 [hp_X]/mL liquid, listed with the FDA by Uriel Pharmacy, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Oxalis acetosella leaf, Formica rufa.

Uriel Pharmacy, Inc, NDC labeler code 48951. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Formica Oxalis?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Formica Oxalis NDC 48951-4203 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-4203Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-4203Add 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
48951-4203-3	4895142030348951420303	60 mL in 1 BOTTLE, DROPPER (48951-4203-3)Marketed from Sep 1, 2009

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): Formica Oxalis
Generic name (nonproprietary): formica oxalis
Active ingredients: Oxalis acetosella leaf — 3 [hp_X]/mLFormica rufa — 5 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Uriel Pharmacy, IncNDC labeler code 48951
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 1, 2009
Listing expires: Dec 31, 2027
Identifiers: Product ID 48951-4203_5d1997e3-80f7-7c9c-e063-6294a90a6df0SPL ID 5d1997e3-80f7-7c9c-e063-6294a90a6df0

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

N448951420303 followed by a unit qualifier and the quantity

Package 48951-4203-03. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 48951-4203

What is NDC 48951-4203?: 48951-4203 is the product NDC for Formica Oxalis, Oxalis acetosella leaf 3 [hp_X]/mL; Formica rufa 5 [hp_X]/mL liquid, listed with the FDA by Uriel Pharmacy, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Formica Oxalis.
What is the active ingredient?: Oxalis acetosella leaf, Formica rufa.
Who is the labeler?: Uriel Pharmacy, Inc, NDC labeler code 48951. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Formica Oxalis?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.