NDC codes

FDA NDC Directory
Product NDC (as listed)80353-900Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80353-0900Add 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
80353-900-01803530900011 CAPSULE in 1 BOTTLE, GLASS (80353-900-01) / 60 CAPSULE in 1 CAPSULE (80353-900-02)Marketed from Dec 7, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Uricozen
Generic name (nonproprietary)
gout recovery, joint pain and inflammation relief, and gout crystal dissolution
Active ingredients
Lonicera japonica flower — 1 [hp_X]/1Portulaca oleracea whole — 1 [hp_X]/1Wolfiporia cocos whole — 1 [hp_X]/1
Dosage form
Capsule
Route
Oral
Labeler
HCBIOPHARMNDC labeler code 80353
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 80353-900_4e3936d2-03a5-6a63-e063-6394a90ad1b9SPL ID 4e3936d2-03a5-6a63-e063-6394a90ad1b9SPL set ID 0bfb4b71-8392-15fa-e063-6394a90a771bUNII 4465L2WS4Y, D5J3623SV2, Y1I7Z6FF4R

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

N480353090001 followed by a unit qualifier and the quantity

Package 80353-0900-01. 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)

To recover from gout* To dissolve gout crystals* To relieve joint pain and joint inflammation*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80353-900

What is NDC 80353-900?
80353-900 is the product NDC for Uricozen, Lonicera japonica flower 1 [hp_X]/1 + 2 more ingredients capsule, listed with the FDA by HCBIOPHARM. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Uricozen (Gout recovery, Joint pain and inflammation relief, and gout crystal dissolution).
What is the active ingredient?
Lonicera japonica flower, Portulaca oleracea whole, Wolfiporia cocos whole.
Who is the labeler?
HCBIOPHARM, NDC labeler code 80353. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Uricozen?
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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