Bryophyllum Avena NDC 48951-2137

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-2137Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-2137Add 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
48951-2137-3	48951213703	60 mL in 1 BOTTLE, DROPPER (48951-2137-3)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): Bryophyllum Avena
Generic name (nonproprietary): bryophyllum avena
Active ingredients: Oat — 3 [hp_X]/mLValerian — 3 [hp_X]/mLOyster shell calcium carbonate, Crude — 7 [hp_X]/mLPhosphorus — 30 [hp_X]/mLSulfur — 30 [hp_X]/mLKalanchoe daigremontiana leaf — 1 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Uriel Pharmacy Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 1, 2009
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Grain Proteins (EXT)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 48951-2137_36393701-e4d5-153e-e063-6294a90ad80bSPL ID 36393701-e4d5-153e-e063-6294a90ad80bSPL set ID f3d21630-0a99-11df-8a39-0800200c9a66UNII Z6J799EAJK, JWF5YAW3QW, 2E32821G6I, 27YLU75U4W, 70FD1KFU70, L6X13JKL8O
Pharmacologic class: Non-Standardized Food 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

N448951213703 followed by a unit qualifier and the quantity

Package 48951-2137-03. 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 May 28, 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)