Allergy Relief
- Product NDC
- 72090-059
- 11-digit product format
- 720900059
- Labeler code
- 72090
- Product ID
- 72090-059_10617e6f-d985-4db4-b0ba-5890a11070b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Pioneer Life Sciences, LLC
- Application
- ANDA209274
- Marketing category
- ANDA
- Marketing start
- 2020-09-21
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72090-059-20 | Allergy Relief | 200 in 1 BOTTLE | TABLET | 200 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72090-059 | ALLERGY RELIEF (CETIRIZINE HCL) TABLET [PIONEER LIFE SCIENCES, LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240522_b064f4ba-d5ff-c503-e053-2995a90ab1ec.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72090-059-20 | 72090005920 | 200 TABLET in 1 BOTTLE (72090-059-20) | 200 tablet | 2020-09-21 | 0000-00-00 | No | No | Current |