NDC 0113-0503-01 - Good Sense Childrens All Day Allergy
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0113-0503
- Requested NDC
- 0113-0503-01
- Package NDCs from labels
- 0113-0503-26, 0113-0503-01, 0113-0503-34
- Manufacturer
- L. Perrigo Company
- Effective date
- 2026-04-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Good Sense Childrens All Day Allergy - L. Perrigo Company | L. Perrigo Company | 2026-04-20 | HUMAN OTC DRUG LABEL |
| Perrigo Children’s All Day Allergy Drug Facts | Preferred Pharmaceuticals Inc. | 2026-03-17 | HUMAN OTC DRUG LABEL |
| Good Sense Childrens All Day Allergy - A-S Medication Solutions | A-S Medication Solutions | 2026-03-04 | HUMAN OTC DRUG LABEL |
| Dye Free Children's Cetirizine Hydrochloride Oral Solution | Precision Dose, Inc. | 2025-02-12 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0113-0503-01 | Good Sense Childrens All Day Allergy | 240 mL in 1 BOTTLE | SOLUTION | 240 | 4 | |
| 0113-0503-26 | Good Sense Childrens All Day Allergy | 1 in 1 CARTON | SOLUTION | 1 | 4 | |
| 0113-0503-26 | Good Sense Childrens All Day Allergy | 118 mL in 1 BOTTLE | SOLUTION | 118 | 4 | |
| 0113-0503-34 | Good Sense Childrens All Day Allergy | 1 in 1 CARTON | SOLUTION | 1 | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0113-0503-26 | ML - Milliliter | 0113-0503 | 274a9c29-2d55-483e-9335-8f112c6b3723 | 1 | 2017-08-11 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.