NDC codes

FDA NDC Directory
Product NDC (as listed)52654-0007Labeler and product segments. Claims need a package NDC.
Product NDC at billing width52654-0007Add 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 NDC11-digit (billing)PackageCopy
52654-0007-152654000701120 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

N452654000701 followed by a unit qualifier and the quantity

Package 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.

Full label on DailyMed (opens in a new tab)

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.

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