Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Mp NDC 52654-0007
Berberis vulgaris root bark 32 [hp_X]/mL + 6 more ingredients · Liquid · Oral · Chi Research, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 52654-0007-1 | 52654000701 | 120 mL in 1 BOTTLE, DROPPER (52654-0007-1)Marketed from Mar 3, 2020 |
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)
- Mp
- Generic name (nonproprietary)
- berberis vulgaris, isatis tinctoria, morinda citrifolia, petiveria tetrandra, schinus molle, thymolum, uva-ursi
- Active ingredients
- Berberis vulgaris root bark — 32 [hp_X]/mLIsatis tinctoria whole — 32 [hp_X]/mLNoni fruit juice — 32 [hp_X]/mLPetiveria alliacea root — 32 [hp_X]/mLSchinus molle fruiting top — 32 [hp_X]/mLThymol — 32 [hp_X]/mLArctostaphylos uva-ursi leaf — 32 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Chi Research, Inc.NDC labeler code 52654
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 52654-0007_2d6c2f7b-a06a-4591-a5f7-211354417e94SPL ID 2d6c2f7b-a06a-4591-a5f7-211354417e94SPL set ID 4b8bb332-a718-47a9-970d-299324309beeUNII 1TH8Q20J0U, T538276W1L, 6ULF85Z07J, D3E2DRD55N, T8L6O1KSB4, 3J50XA376E, 3M5V3D1X36
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
N452654000701followed by a unit qualifier and the quantityPackage 52654-0007-01. 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 .
Indications (excerpt from the label)
INDICATIONS: For temporary relief of symptoms of respiratory discomfort.
Excerpt only. Read the full label for complete information.
About NDC 52654-0007
- What is NDC 52654-0007?
- 52654-0007 is the product NDC for Mp, Berberis vulgaris root bark 32 [hp_X]/mL + 6 more ingredients liquid, listed with the FDA by Chi Research, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Mp (Berberis Vulgaris, Isatis Tinctoria, Morinda Citrifolia, Petiveria Tetrandra, Schinus Molle, Thymolum, Uva-Ursi).
- What is the active ingredient?
- Berberis vulgaris root bark, Isatis tinctoria whole, Noni fruit juice, Petiveria alliacea root, Schinus molle fruiting top, Thymol, Arctostaphylos uva-ursi leaf.
- Who is the labeler?
- Chi Research, Inc., NDC labeler code 52654. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Mp?
- 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.