NDC codes

FDA NDC Directory
Product NDC (as listed)63083-2122Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63083-2122Add 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
63083-2122-2630832122026308321220259 mL in 1 BOTTLE, DROPPER (63083-2122-2)Marketed from Aug 15, 1985

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)
Urinary Tract Drops 2122Suffix: 2122
Generic name (nonproprietary)
urinary tract drops
Active ingredients
Crateva magna bark — 3 [hp_X]/59mLAgathosma betulina leaf — 6 [hp_X]/59mLSus scrofa urinary bladder — 6 [hp_X]/59mLEquisetum arvense top — 6 [hp_X]/59mLBeef kidney — 6 [hp_X]/59mLToxicodendron pubescens leaf — 12 [hp_X]/59mLSepia officinalis juice — 60 [hp_X]/59mLDelphinium staphisagria seed — 60 [hp_X]/59mLLytta vesicatoria — 12 [hp_X]/59mLSmilax ornata root — 12 [hp_X]/59mLCausticum — 30 [hp_X]/59mLChimaphila umbellata whole — 30 [hp_X]/59mLUrtica urens whole — 30 [hp_X]/59mL
Dosage form
Liquid
Route
Oral
Labeler
Professional Complementary Health FormulasNDC labeler code 63083
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 63083-2122_6d4accd2-7cde-4299-8316-2110b1971291SPL ID 6d4accd2-7cde-4299-8316-2110b1971291SPL set ID 0373cd9c-73d5-4994-94ef-fe7084b633f6UNII RS704ZO5ZL, 369DDH39Z0, 3G7U72W8DA, 1DP6Y6B65Z, 5HOC10FSIC, 6IO182RP7A, QDL83WN8C2, 00543AP1JV, 3Q034RO3BT, 2H1576D5WG, DD5FO1WKFU, WCK21A9W9J, IHN2NQ5OF9

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

N463083212202 followed by a unit qualifier and the quantity

Package 63083-2122-02. 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)

INDICATIONS For the temporary relief of urinary discomfort or difficulty, frequent urination, or mild abdominal or back pain.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-2122

What is NDC 63083-2122?
63083-2122 is the product NDC for Urinary Tract Drops 2122 (urinary tract drops), Crateva magna bark 3 [hp_X]/59mL + 12 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Urinary Tract Drops 2122 (Urinary Tract Drops).
What is the active ingredient?
Crateva magna bark, Agathosma betulina leaf, Sus scrofa urinary bladder, Equisetum arvense top, Beef kidney, Toxicodendron pubescens leaf, Sepia officinalis juice, Delphinium staphisagria seed, Lytta vesicatoria, Smilax ornata root, Causticum, Chimaphila umbellata whole, Urtica urens whole.
Who is the labeler?
Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Urinary Tract Drops 2122?
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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