NDC codes

FDA NDC Directory
Product NDC (as listed)53209-5001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width53209-5001Add 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
53209-5001-153209500101532095001011 TABLET, FILM COATED in 1 BLISTER PACK (53209-5001-1)Marketed from Jun 19, 2025

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)
Zyrtec Allergy
Generic name (nonproprietary)
cetirizine hydrochloride
Active ingredients
Cetirizine hydrochloride — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Morning Star OTCNDC labeler code 53209
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 53209-5001_37e96646-1587-1156-e063-6394a90a6b22SPL ID 37e96646-1587-1156-e063-6394a90a6b22SPL set ID 3efa421d-ea70-4b1f-95d0-7c63b6c39580RxCUI 1014678, 1020026UNII 64O047KTOA
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

N453209500101 followed by a unit qualifier and the quantity

Package 53209-5001-01. 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)

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.

Full label on DailyMed (opens in a new tab)

About NDC 53209-5001

What is NDC 53209-5001?
53209-5001 is the product NDC for Zyrtec Allergy (cetirizine hydrochloride), Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Morning Star OTC. It has 1 package NDC, 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?
Morning Star OTC, NDC labeler code 53209. 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.

Other finished products listed under the same name: strengths, forms and labelers.

Other Zyrtec Allergy NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralSavings Distributors LLC73097-01673097-0016-20
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 5 mg/1Tablet, Film coatedOralKenvue Brands LLC50580-75450580-0754-1550580-0754-35
ZYRTEC Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Capsule, Liquid filledOralKenvue Brands LLC50580-78650580-0786-1250580-0786-1350580-0786-25+5 more
Zyrtec Allergycetirizine hydrochloride—KitKenvue Brands LLC50580-75250580-0752-01
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralNavajo Manufacturing Company Incorporated67751-19267751-0192-01
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralKenvue Brands LLC50580-77850580-0778-24
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralKenvue Brands LLC50580-72650580-0726-0350580-0726-0550580-0726-25+19 more
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralRedPharm Drug Inc67296-148467296-1484-03
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralSelect Consumer Group85237-296085237-2960-0185237-2960-03

Other NDCs under NDA 019835

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 019835
ProductStrengthForm · routeLabelerProduct NDC
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralKenvue Brands LLC50580-726
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 5 mg/1Tablet, Film coatedOralKenvue Brands LLC50580-754
Zyrtec Allergycetirizine hydrochloride—KitKenvue Brands LLC50580-752
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralRedPharm Drug Inc67296-1484
Zyrtec Allergy, Lil Drug Storecetirizine hydrochloride tablet, film coatedCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralLil' Drug Store Products, Inc.66715-9811
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralSavings Distributors LLC73097-016
ZYRTEC Hivescetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralKenvue Brands LLC50580-116
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralNavajo Manufacturing Company Incorporated67751-192
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralSelect Consumer Group85237-2960

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