What is NDC 48951-8125?

48951-8125 is the product NDC for Renes Betula, Elymus repens root 4 [hp_X]/mL + 11 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?

Elymus repens root, Ononis repens root, Parsley, Capsella bursa-pastoris, Arctostaphylos uva-ursi leaf, Solidago virgaurea flowering top, Betula pubescens leaf, Equisetum arvense top, Pork kidney, Cytisus scoparius flowering top, Copper, Petroselinum crispum root.

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 Renes Betula?

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.

Renes Betula NDC 48951-8125 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-8125Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-8125Add 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
48951-8125-3	4895181250348951812503	60 mL in 1 BOTTLE, DROPPER (48951-8125-3)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): Renes Betula
Generic name (nonproprietary): renes betula
Active ingredients: Elymus repens root — 4 [hp_X]/mLOnonis repens root — 2 [hp_X]/mLParsley — 2 [hp_X]/mLCapsella bursa-pastoris — 2 [hp_X]/mLArctostaphylos uva-ursi leaf — 2 [hp_X]/mLSolidago virgaurea flowering top — 2 [hp_X]/mLBetula pubescens leaf — 4 [hp_X]/mLEquisetum arvense top — 3 [hp_X]/mLPork kidney — 6 [hp_X]/mLCytisus scoparius flowering top — 3 [hp_X]/mLCopper — 8 [hp_X]/mLPetroselinum crispum root — 2 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Uriel Pharmacy Inc.NDC labeler code 48951
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 1, 2009
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 48951-8125_53eccc8d-5910-3869-e063-6294a90ac2d1SPL ID 53eccc8d-5910-3869-e063-6294a90ac2d1SPL set ID e7c64fc1-3e3b-478f-8b7b-c1a2b7780ba5UNII 3IXW0F6P8W, W06YCM9T44, 58FMD0Q0EV, W0X9457M59, 3M5V3D1X36, 5405K23S50, 84SOH0O3OO, 1DP6Y6B65Z, X7BCI5P86H, XZC6H8R666, 789U1901C5, 030FN29S9H
Pharmacologic class: Copper-containing Intrauterine Device; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N448951812503 followed by a unit qualifier and the quantity

Package 48951-8125-03. 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 Jun 10, 2026.

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 48951-8125

What is NDC 48951-8125?: 48951-8125 is the product NDC for Renes Betula, Elymus repens root 4 [hp_X]/mL + 11 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?: Renes Betula.
What is the active ingredient?: Elymus repens root, Ononis repens root, Parsley, Capsella bursa-pastoris, Arctostaphylos uva-ursi leaf, Solidago virgaurea flowering top, Betula pubescens leaf, Equisetum arvense top, Pork kidney, Cytisus scoparius flowering top, Copper, Petroselinum crispum root.
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 Renes Betula?: 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.