childrens allergy relief
- Product NDC
- 21130-653
- 11-digit product format
- 211300653
- Labeler code
- 21130
- Product ID
- 21130-653_14ab13cb-7eca-40cd-8eb1-4933676e091b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- cetirizine hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Safeway
- Application
- ANDA204226
- Marketing category
- ANDA
- Marketing start
- 2024-04-03
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- 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 |
|---|
| 21130-653-26 | 21130065326 | 1 BOTTLE in 1 CARTON (21130-653-26) / 120 mL in 1 BOTTLE | 1 bottle | 2024-04-03 | No | No | Historical |