Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Lycopodium Berberis NDC 48951-6049
Milk thistle 1 [hp_X]/1 + 8 more ingredients · Pellet · Oral · Uriel Pharmacy Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 48951-6049-2 | 4895160490248951604902 | 1350 PELLET in 1 BOTTLE, GLASS (48951-6049-2)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)
- Lycopodium Berberis
- Generic name (nonproprietary)
- lycopodium berberis
- Active ingredients
- Milk thistle — 1 [hp_X]/1Berberis vulgaris root bark — 3 [hp_X]/1Lycopodium clavatum spore — 3 [hp_X]/1Chelidonium majus root — 5 [hp_X]/1Turmeric — 5 [hp_X]/1Fragaria vesca whole — 5 [hp_X]/1Vitis vinifera leaf — 5 [hp_X]/1Sulfide ion — 6 [hp_X]/1Calomel — 10 [hp_X]/1
- Dosage form
- Pellet
- Route
- Oral
- Labeler
- Uriel Pharmacy Inc.NDC labeler code 48951
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 48951-6049_426390c8-1157-e3af-e063-6394a90a340bSPL ID 426390c8-1157-e3af-e063-6394a90a340bSPL set ID 8312ff6b-4d20-41d4-b736-b50c081c64b6UNII U946SH95EE, 1TH8Q20J0U, C88X29Y479, FLT36UCF0N, 856YO1Z64F, 5J340B7H82, R1H893D80E, G15I91XETI, J2D46N657D
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
N448951604902followed by a unit qualifier and the quantityPackage 48951-6049-02. 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 .
Indications (excerpt from the label)
Directions: FOR ORAL USE ONLY.
Excerpt only. Read the full label for complete information.
About NDC 48951-6049
- What is NDC 48951-6049?
- 48951-6049 is the product NDC for Lycopodium Berberis, Milk thistle 1 [hp_X]/1 + 8 more ingredients pellet, 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?
- Lycopodium Berberis.
- What is the active ingredient?
- Milk thistle, Berberis vulgaris root bark, Lycopodium clavatum spore, Chelidonium majus root, Turmeric, Fragaria vesca whole, Vitis vinifera leaf, Sulfide ion, Calomel.
- 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 Lycopodium Berberis?
- 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.