CHILDRENS ZYRTEC
- Product NDC
- 50090-6781
- 11-digit product format
- 500906781
- Labeler code
- 50090
- Product ID
- 50090-6781_b5000f03-33a3-48ae-b0bf-66a3c52c50af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine hydrochloride
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA021621
- Marketing category
- NDA
- Marketing start
- 2021-06-21
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 64O047KTOA | CETIRIZINE HYDROCHLORIDE | 83881-52-1 | CETIRIZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6781-0 | 50090678100 | 4 BLISTER PACK in 1 CARTON (50090-6781-0) / 6 TABLET, CHEWABLE in 1 BLISTER PACK | 4 blister pack | 2023-10-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| CHILDRENS ZYRTEC | A-S Medication Solutions | 2025-03-03 | HUMAN OTC DRUG LABEL | 3 |