Allergy Relief
- Product NDC
- 37808-106
- 11-digit product format
- 378080106
- Labeler code
- 37808
- Product ID
- 37808-106_3e05caf8-84cf-478f-9401-762f51c9e796
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA201546
- Marketing category
- ANDA
- Marketing start
- 2011-05-20
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- 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 | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 64O047KTOA |
| Rxcui | 1014673 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-106-08 | Allergy Relief | 120 mL in 1 BOTTLE | SOLUTION | 120 | | 2 |
| 37808-106-08 | Allergy Relief | 1 in 1 CARTON | SOLUTION | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-106 | ALLERGY RELIEF (CETIRIZINE HYDROCHLORIDE) SOLUTION [H E B] | 2 | Current NDC, Legacy NDC, 2 package rows | 20180512_fdd3f9a0-b4be-498a-b8e0-1a9740399736.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 |
|---|
| 37808-106-08 | 37808010608 | 1 BOTTLE in 1 CARTON (37808-106-08) / 120 mL in 1 BOTTLE | 1 bottle | 2018-04-12 | 0000-00-00 | No | No | Current |