All Day Allergy Relief
- Product NDC
- 55910-269
- 11-digit product format
- 559100269
- Labeler code
- 55910
- Product ID
- 55910-269_0c774d83-58dd-d9b3-e063-6394a90a6f7a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DOLGENCORP, INC.
- Application
- ANDA078933
- Marketing category
- ANDA
- Marketing start
- 2023-12-20
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- All Day Allergy Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CETIRIZINE HYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 64O047KTOA |
| Rxcui | 1014678 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55910-269-58 | All Day Allergy Relief | 1 in 1 CARTON | TABLET | 1 | | 2 |
| 55910-269-58 | All Day Allergy Relief | 45 in 1 BOTTLE | TABLET | 45 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55910-269 | ALL DAY ALLERGY RELIEF (CETIRIZINE HYDROCHLORIDE) TABLET [DOLGENCORP, INC.] | 2 | Current NDC, 2 package rows | 20231220_0643ea78-9709-8526-e063-6394a90a227b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55910-269-58 | 55910026958 | 1 BOTTLE in 1 CARTON (55910-269-58) / 45 TABLET in 1 BOTTLE | 1 bottle | 2023-12-20 | No | No | Historical |