What is NDC 48951-3088?

48951-3088 is the product NDC for Chrysosplenium Chamomilla, Matricaria recutita 3 [hp_X]/mL + 3 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?

Matricaria recutita, Chrysosplenetin, Cichorium intybus whole, Taraxacum palustre 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 Chrysosplenium Chamomilla?

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.

Chrysosplenium Chamomilla NDC 48951-3088

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-3088Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-3088Add 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
48951-3088-1	4895130880148951308801	10 AMPULE in 1 BOX (48951-3088-1) / 1 mL in 1 AMPULEMarketed 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): Chrysosplenium Chamomilla
Generic name (nonproprietary): chrysosplenium chamomilla
Active ingredients: Matricaria recutita — 3 [hp_X]/mLChrysosplenetin — 3 [hp_X]/mLCichorium intybus whole — 6 [hp_X]/mLTaraxacum palustre root — 6 [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
Identifiers: Product ID 48951-3088_4bd3ab6e-a571-75f6-e063-6394a90a9f3aSPL ID 4bd3ab6e-a571-75f6-e063-6394a90a9f3aSPL set ID d2c9746c-784b-4d76-874b-4f8ea6814f99UNII G0R4UBI2ZZ, 9AA5Z8PMYE, 1KE45XD28S, GCZ4W7077C

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

N448951308801 followed by a unit qualifier and the quantity

Package 48951-3088-01. 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 Feb 27, 2026.

Indications (excerpt from the label)

FOR ORAL USE ONLY

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 48951-3088

What is NDC 48951-3088?: 48951-3088 is the product NDC for Chrysosplenium Chamomilla, Matricaria recutita 3 [hp_X]/mL + 3 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?: Chrysosplenium Chamomilla.
What is the active ingredient?: Matricaria recutita, Chrysosplenetin, Cichorium intybus whole, Taraxacum palustre 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 Chrysosplenium Chamomilla?: 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.