What is NDC 48951-9389?

48951-9389 is the product NDC for Uva ursi comp., Arctostaphylos uva-ursi leaf 1 [hp_X]/mL + 4 more ingredients 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?

Arctostaphylos uva-ursi leaf, Wormwood, Berberis vulgaris root bark, Lytta vesicatoria, Larix decidua resin.

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 Uva ursi comp.?

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.

Uva ursi comp. NDC 48951-9389 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-9389Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-9389Add 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
48951-9389-3	4895193890348951938903	60 mL in 1 BOTTLE, DROPPER (48951-9389-3)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): Uva ursi comp.
Generic name (nonproprietary): uva ursi comp.
Active ingredients: Arctostaphylos uva-ursi leaf — 1 [hp_X]/mLWormwood — 1 [hp_X]/mLBerberis vulgaris root bark — 1 [hp_X]/mLLytta vesicatoria — 2 [hp_X]/mLLarix decidua resin — 3 [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, 2026
Identifiers: Product ID 48951-9389_2c280a05-da88-0480-e063-6294a90a9502SPL ID 2c280a05-da88-0480-e063-6294a90a9502SPL set ID 2c280a05-da87-0480-e063-6294a90a9502UNII 3M5V3D1X36, F84709P2XV, 1TH8Q20J0U, 3Q034RO3BT, AD8LJ73GQF

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

N448951938903 followed by a unit qualifier and the quantity

Package 48951-9389-03. 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

Current FDA label (SPL), effective Jan 20, 2025.

Indications (excerpt from the label)

Directions: FOR ORAL USE ONLY.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 48951-9389

What is NDC 48951-9389?: 48951-9389 is the product NDC for Uva ursi comp., Arctostaphylos uva-ursi leaf 1 [hp_X]/mL + 4 more ingredients 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?: Uva ursi comp..
What is the active ingredient?: Arctostaphylos uva-ursi leaf, Wormwood, Berberis vulgaris root bark, Lytta vesicatoria, Larix decidua resin.
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 Uva ursi comp.?: 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.