all day relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by H.j. Harkins Company, Inc.. The primary component is Naproxen Sodium.
| Product ID | 52959-469_2f8a9fb7-d0df-4362-a206-38c6a4291fd6 |
| NDC | 52959-469 |
| Product Type | Human Otc Drug |
| Proprietary Name | all day relief |
| Generic Name | Naproxen Sodium |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1997-01-09 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA074661 |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | NAPROXEN SODIUM |
| Active Ingredient Strength | 220 mg/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 1997-01-09 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-09 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-09 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-09 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-09 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-09 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-09 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-09 |
| Inactivation Date | 2019-11-13 |
| Ingredient | Strength |
|---|---|
| NAPROXEN SODIUM | 220 mg/1 |
| SPL SET ID: | bc79612a-1db4-457f-8e15-0c7659c34c2a |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 68788-9971 | All Day Relief | All Day Relief |
| 0536-1023 | All Day Relief | All Day Relief |
| 0536-1022 | All Day Relief | All Day Relief |
| 42507-368 | all day relief | all day relief |
| 42507-140 | all day relief | all day relief |
| 52959-469 | all day relief | all day relief |
| 56062-490 | all day relief | all day relief |
| 56062-368 | All Day Relief | All Day Relief |
| 56062-748 | All Day Relief | All Day Relief |
| 0280-6000 | Aleve | NAPROXEN SODIUM |
| 0280-6010 | Aleve | NAPROXEN SODIUM |
| 0280-6020 | Aleve | NAPROXEN SODIUM |
| 0280-0041 | Aleve Headache Pain | Naproxen Sodium |
| 0113-7033 | basic care naproxen sodium | Naproxen Sodium |
| 0113-7368 | Basic Care Naproxen Sodium | Naproxen Sodium |
| 0113-7901 | basic care naproxen sodium | Naproxen Sodium |
| 0113-0901 | Good Sense Naproxen Sodium | Naproxen Sodium |
| 0113-1412 | good sense naproxen sodium | naproxen sodium |
| 0113-1773 | good sense naproxen sodium | Naproxen Sodium |
| 0113-4368 | Good Sense Naproxen Sodium | Naproxen Sodium |
| 0280-0270 | Menstridol | NAPROXEN SODIUM |
| 0143-9908 | NAPROXEN | naproxen sodium |
| 0143-9916 | NAPROXEN | naproxen sodium |