Over-the-counter drug · NDA
Zyrtec Allergy (Cetirizine hydrochloride) NDC 50580-726
Cetirizine hydrochloride 10 mg/1 · Tablet, Film coated · Oral · Kenvue Brands LLC
NDC codes
FDA NDC DirectoryProduct NDC (as listed)50580-726Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50580-0726Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50580-726-03 | 5058007260350580072603 | 50 BLISTER PACK in 1 CARTON (50580-726-03) / 1 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Jan 1, 2008 | |
| 50580-726-05 | 5058007260550580072605 | 50 POUCH in 1 CARTON (50580-726-05) / 1 TABLET, FILM COATED in 1 POUCHMarketed from Mar 1, 2023 | |
| 50580-726-25 | 5058007262550580072625 | 2500 POUCH in 1 CASE (50580-726-25) / 1 TABLET, FILM COATED in 1 POUCHMarketed from Mar 1, 2023 | |
| 50580-726-36 | 5058007263650580072636 | 1 BOTTLE, PLASTIC in 1 PACKAGE (50580-726-36) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Jan 1, 2008 | |
| 50580-726-40 | 5058007264050580072640 | 1 BOTTLE, PLASTIC in 1 PACKAGE (50580-726-40) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Jan 20, 2014 | |
| 50580-726-45 | 5058007264550580072645 | 1 BOTTLE in 1 CARTON (50580-726-45) / 45 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 31, 2025 | |
| 50580-726-50 | 5058007265050580072650 | 1 BOTTLE, PLASTIC in 1 PACKAGE (50580-726-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Jan 26, 2010 | |
| 50580-726-66 | 5058007266650580072666 | 75 TABLET, FILM COATED in 1 PACKAGE, COMBINATION (50580-726-66)Marketed from Jan 1, 2008 | |
| 50580-726-70 | 5058007267050580072670 | 1 BOTTLE, PLASTIC in 1 PACKAGE (50580-726-70) / 70 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Jan 1, 2008 | |
| 50580-726-71 | 5058007267150580072671 | 1 BOTTLE in 1 CARTON (50580-726-71) / 30 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 1, 2024 | |
| 50580-726-72 | 5058007267250580072672 | 1 BOTTLE in 1 CARTON (50580-726-72) / 40 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 1, 2024 | |
| 50580-726-73 | 5058007267350580072673 | 1 BOTTLE in 1 CARTON (50580-726-73) / 60 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 1, 2024 | |
| 50580-726-74 | 5058007267450580072674 | 1 BOTTLE in 1 CARTON (50580-726-74) / 90 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 1, 2024 | |
| 50580-726-75 | 5058007267550580072675 | 1 BOTTLE in 1 CARTON (50580-726-75) / 75 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 31, 2025 | |
| 50580-726-90 | 5058007269050580072690 | 2 BOTTLE, PLASTIC in 1 PACKAGE (50580-726-90) / 45 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Jan 26, 2010 | |
| 50580-726-91 | 5058007269150580072691 | 2500 POUCH in 1 CARTON (50580-726-91) / 1 TABLET, FILM COATED in 1 POUCHMarketed from Jul 27, 2018 | |
| 50580-726-92 | 5058007269250580072692 | 50 POUCH in 1 TRAY (50580-726-92) / 1 TABLET, FILM COATED in 1 POUCHMarketed from Jul 12, 2018 | |
| 50580-726-93 | 5058007269350580072693 | 3 POUCH in 1 CARTON (50580-726-93) / 1 TABLET, FILM COATED in 1 POUCHMarketed from Jul 27, 2018 | |
| 50580-726-94 | 5058007269450580072694 | 1 BOTTLE in 1 PACKAGE (50580-726-94) / 60 TABLET, FILM COATED in 1 BOTTLEMarketed from Jun 15, 2020 | |
| 50580-726-95 | 5058007269550580072695 | 1 BOTTLE in 1 PACKAGE (50580-726-95) / 90 TABLET, FILM COATED in 1 BOTTLEMarketed from Jun 15, 2020 | |
| 50580-726-96 | 5058007269650580072696 | 5 POUCH in 1 CARTON (50580-726-96) / 1 TABLET, FILM COATED in 1 POUCHMarketed from May 30, 2020 | |
| 50580-726-97 | 5058007269750580072697 | 14 POUCH in 1 CARTON (50580-726-97) / 1 TABLET, FILM COATED in 1 POUCHMarketed from May 30, 2020 |
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)
- Zyrtec Allergy
- Generic name (nonproprietary)
- cetirizine hydrochloride
- Active ingredients
- Cetirizine hydrochloride — 10 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Kenvue Brands LLCNDC labeler code 50580
- Product type
- Over-the-counter drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 019835
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H1 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 50580-726_40cb0300-d3f3-4a66-e063-6394a90a41dcSPL ID 40cb0300-d3f3-4a66-e063-6394a90a41dcSPL set ID b165db38-b302-4220-8627-77cb07bb078cRxCUI 1014678, 1020026UNII 64O047KTOAUPC 0312547204361
- Pharmacologic class
- Histamine-1 Receptor Antagonist
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
N450580072603followed by a unit qualifier and the quantityPackage 50580-0726-03. 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)
Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat
Excerpt only. Read the full label for complete information.
About NDC 50580-726
- What is NDC 50580-726?
- 50580-726 is the product NDC for Zyrtec Allergy (cetirizine hydrochloride), Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Kenvue Brands LLC. It has 22 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Zyrtec Allergy (Cetirizine Hydrochloride).
- What is the active ingredient?
- Cetirizine hydrochloride.
- Who is the labeler?
- Kenvue Brands LLC, NDC labeler code 50580. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Zyrtec Allergy?
- 9 other product NDCs are listed under this name. See all Zyrtec Allergy NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Zyrtec Allergy products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Savings Distributors LLC | 73097-016 | 73097-0016-20 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Morning Star OTC | 53209-5001 | 53209-5001-01 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 5 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-754 | 50580-0754-1550580-0754-35 |
| ZYRTEC Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Capsule, Liquid filledOral | Kenvue Brands LLC | 50580-786 | 50580-0786-1250580-0786-1350580-0786-25+5 more |
| Zyrtec Allergycetirizine hydrochloride | — | Kit | Kenvue Brands LLC | 50580-752 | 50580-0752-01 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Navajo Manufacturing Company Incorporated | 67751-192 | 67751-0192-01 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Orally disintegratingOral | Kenvue Brands LLC | 50580-778 | 50580-0778-24 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | RedPharm Drug Inc | 67296-1484 | 67296-1484-03 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Select Consumer Group | 85237-2960 | 85237-2960-0185237-2960-03 |
Other NDCs under NDA 019835
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 5 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-754 |
| Zyrtec Allergycetirizine hydrochloride | — | Kit | Kenvue Brands LLC | 50580-752 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | RedPharm Drug Inc | 67296-1484 |
| Zyrtec Allergy, Lil Drug Storecetirizine hydrochloride tablet, film coated | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Lil' Drug Store Products, Inc. | 66715-9811 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Savings Distributors LLC | 73097-016 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Morning Star OTC | 53209-5001 |
| ZYRTEC Hivescetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-116 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Navajo Manufacturing Company Incorporated | 67751-192 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Select Consumer Group | 85237-2960 |