Allergy Relief
- Product NDC
- 81522-192
- 11-digit product format
- 815220192
- Labeler code
- 81522
- Product ID
- 81522-192_2fc2551f-18bf-99de-e063-6394a90a6523
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- FSA STORE INC.
- Application
- ANDA211075
- Marketing category
- ANDA
- Marketing start
- 2025-01-01
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 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 |
|---|
| FEXOFENADINE HYDROCHLORIDE | 180 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2S068B75ZU |
| Rxcui | 997420 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81522-192-09 | Allergy Relief | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 2 |
| 81522-192-09 | Allergy Relief | 1 in 1 PACKAGE | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81522-192 | ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE) TABLET [FSA STORE INC.] | 2 | Current NDC, 2 package rows | 20250309_276e9767-93c0-5932-e063-6394a90ab2d9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 81522-192-09 | 81522019209 | 1 BOTTLE, PLASTIC in 1 PACKAGE (81522-192-09) / 90 TABLET in 1 BOTTLE, PLASTIC | 2025-01-01 | No | No | Historical |