Zyrtec 2s Blister, 2 Tablets per Blister, 6 Blisters per Box

Manufacturer
JC World Bell Wholesale Co., Inc. | Kenvue Brands LLC
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:50:05

Label at a glance#

ProductZyrtec 2s Blister
Active ingredientCETIRIZINE HYDROCHLORIDE
Label structure8 sections

Indications and 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

Dosage and administration

 adults and children 6 years and over one 10mg tablet  once daily; do not take more than one 10mg tabelt in 24 hours. A 5 mg product may be appropriate for less severe symptoms. adults 65 years and over  ask a doctor children under 6 years of age  ask a doctor consumers with liver or kidney disease  ask a doctor

Label contents#

Full prescribing information#

Active ingredient ((in each tablet)) 

OTC - ACTIVE INGREDIENT SECTION

Cetrizine HCl 10 mg

Purpose

OTC - PURPOSE SECTION

Antihistamine

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

liver or kidny disease. Your doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking tranquilizers or sedatives.

When using this product

OTC - WHEN USING SECTION

  • drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

OTC - STOP USE SECTION

an allergic reastion to this product occurs. Seek medical help right away.

If pregnant or breast-feeding:

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • if breast-feeding: not recommended
  • if pregnant: ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

 adults and children

6 years and over

one 10mg tablet  once daily; do not take more than one 10mg tabelt in 24 hours. A 5 mg product may be appropriate for less severe symptoms.
adults 65 years and over ask a doctor
children under 6 years of age ask a doctor
consumers with liver or kidney disease ask a doctor

Other information

SPL UNCLASSIFIED SECTION

  • store between 20° to 25°C (68° to 77°F)
  • do not use if pouch is torn or damaged
  • meets USP Dissolution Test 2

Inactive ingredients

INACTIVE INGREDIENT SECTION

colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide

Questions?

OTC - QUESTIONS SECTION

call 1-800-343-7805 (toll-free) or 215-273-8755 (collect)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageIneer PackageIneer Package

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1014678cetirizine HCl 10 MG Oral TabletPSN3
1020026ZyrTEC 10 MG Oral TabletPSN3
1020026cetirizine hydrochloride 10 MG Oral Tablet [Zyrtec]SBD3
1014678cetirizine hydrochloride 10 MG Oral TabletSCD3
1014678cetirizine HCl 10 MG Oral TabletSY3
1020026Zyrtec (cetirizine dihydrochloride 10 MG) Oral TabletSY3
1020026Zyrtec 10 MG Oral TabletSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CETIRIZINE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c505bb17-4ff9-45f9-ac2d-bb9c8c9d35beProduct name120200304
a255659f-db40-429d-8c07-5f173f330d9cProduct name120190402

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50269-019-02Zyrtec 2s Blister6 in 1 BOXTABLET, FILM COATED63
50269-019-02Zyrtec 2s Blister2 in 1 BLISTER PACKTABLET, FILM COATED23

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50269-019ZYRTEC 2S BLISTER (CETIRIZINE HYDROCHLORIDE) TABLET, FILM COATED [JC WORLD BELL WHOLESALE CO., INC.]3Legacy NDC, 2 package rows20250101_af0ba7b0-b511-9f81-e053-2a95a90ade2c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50580-726-30EA - Each50580-726853bd501-594a-43ba-8d6e-e570fc3ab76412012-07-24
50580-726-32EA - Each50580-726075b55b7-dbdc-464a-b6a4-6071a07901fc12012-07-24
50580-726-36EA - Each50580-7264159f1d6-19ba-4c79-8ede-b5d73ee883fb12012-07-24
50580-726-38EA - Each50580-7266ad75859-5196-4c44-a976-8da28a0c95e912012-07-24
50580-726-51EA - Each50580-726a2ed8aaf-f19c-4a7e-8aff-41d2a0f3ec9612012-07-24
50580-726-93EA - Each50580-726c0eb6ce2-976c-4e27-af1f-c011ac402eb812018-10-11
50580-726-96EA - Each50580-72682123398-20e6-4b44-bba9-0c664a14a66e12022-08-04

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50269-01950269-019-02
50580-726

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N019835-003ZYRTEC ALLERGYCETIRIZINE HYDROCHLORIDE5MGTABLET / ORALRLD2007-11-16
N019835-004ZYRTEC ALLERGYCETIRIZINE HYDROCHLORIDE10MGTABLET / ORALRLD, RS2007-11-16
N019835-005ZYRTEC HIVESCETIRIZINE HYDROCHLORIDE5MGTABLET / ORALRLD2007-11-16
N019835-006ZYRTEC HIVESCETIRIZINE HYDROCHLORIDE10MGTABLET / ORALRLD2007-11-16

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 5 · 172 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-1684e616aacf4f…
2026-09-14 22:38:342026-08N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-1684e616aacf4f…
2026-09-14 22:38:342026-08N019835-005ZYRTEC HIVES5MGTABLET / ORALRLD2007-11-1684e616aacf4f…
2026-09-14 22:38:342026-08N019835-006ZYRTEC HIVES10MGTABLET / ORALRLD2007-11-1684e616aacf4f…
2026-08-18 06:07:402026-07N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-16caaa826d4ba7…
2026-08-18 06:07:402026-07N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-16caaa826d4ba7…
2026-08-18 06:07:402026-07N019835-005ZYRTEC HIVES5MGTABLET / ORALRLD2007-11-16caaa826d4ba7…
2026-08-18 06:07:402026-07N019835-006ZYRTEC HIVES10MGTABLET / ORALRLD2007-11-16caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-16011fe1cb6892…
2026-02-19 14:30 UTC2026-02N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-16011fe1cb6892…
2026-02-19 14:30 UTC2026-02N019835-005ZYRTEC HIVES5MGTABLET / ORALRLD2007-11-16011fe1cb6892…
2026-02-19 14:30 UTC2026-02N019835-006ZYRTEC HIVES10MGTABLET / ORALRLD2007-11-16011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-1631067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-1631067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N019835-005ZYRTEC HIVES5MGTABLET / ORALRLD2007-11-1631067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N019835-006ZYRTEC HIVES10MGTABLET / ORALRLD2007-11-1631067a03dcf5…
2025-08-23 18:47 UTC2025-08N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-166a471c1ec25d…
2025-08-23 18:47 UTC2025-08N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-166a471c1ec25d…
2025-08-23 18:47 UTC2025-08N019835-005ZYRTEC HIVES5MGTABLET / ORALRLD2007-11-166a471c1ec25d…
2025-08-23 18:47 UTC2025-08N019835-006ZYRTEC HIVES10MGTABLET / ORALRLD2007-11-166a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-16fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-16fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N019835-005ZYRTEC HIVES5MGTABLET / ORALRLD2007-11-16fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N019835-006ZYRTEC HIVES10MGTABLET / ORALRLD2007-11-16fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-16b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-16b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N019835-005ZYRTEC HIVES5MGTABLET / ORALRLD2007-11-16b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N019835-006ZYRTEC HIVES10MGTABLET / ORALRLD2007-11-16b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-1603ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-1603ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N019835-005ZYRTEC HIVES5MGTABLET / ORALRLD2007-11-1603ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N019835-006ZYRTEC HIVES10MGTABLET / ORALRLD2007-11-1603ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-162680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-162680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N019835-005ZYRTEC HIVES RELIEF5MGTABLET / ORALRLD2007-11-162680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N019835-006ZYRTEC HIVES RELIEF10MGTABLET / ORALRLD2007-11-162680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N019835-003ZYRTEC ALLERGY5MGTABLET / ORALRLD2007-11-165bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N019835-004ZYRTEC ALLERGY10MGTABLET / ORALRLD, RS2007-11-165bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N019835-005ZYRTEC HIVES RELIEF5MGTABLET / ORALRLD2007-11-165bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N019835-006ZYRTEC HIVES RELIEF10MGTABLET / ORALRLD2007-11-165bbf6a4d5a75…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Zyrtec AllergyCETIRIZINE HYDROCHLORIDEKenvue Brands LLCb165db38-b302-4220-8627-77cb07bb078c2025-10-10WarningsExact identifier
ndc (product): 50580-726
2a95607f-55a5-2f9a-e063-6394a90ac2dbaf0ba7b0-b511-9f81-e053-2a95a90ade2c2024-12-31WarningsExact identifier
spl id: 2a95607f-55a5-2f9a-e063-6394a90ac2db
spl set id: af0ba7b0-b511-9f81-e053-2a95a90ade2c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.