All Day Pain Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by We Care Distributor Inc.. The primary component is Naproxen Sodium.
| Product ID | 70005-008_b3b4bb86-ef6b-4377-984c-583fd64e7536 | 
| NDC | 70005-008 | 
| Product Type | Human Otc Drug | 
| Proprietary Name | All Day Pain Relief | 
| Generic Name | Naproxen Sodium Tablets, 220 Mg | 
| Dosage Form | Tablet | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2011-09-30 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA091353 | 
| Labeler Name | We Care Distributor Inc. | 
| Substance Name | NAPROXEN SODIUM | 
| Active Ingredient Strength | 220 mg/1 | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2019-12-31 | 
| Marketing Start Date | 2011-09-30 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | ANDA | 
| Application Number | ANDA091353 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2011-09-30 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA091353 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2011-09-30 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA091353 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2011-09-30 | 
| Inactivation Date | 2020-01-31 | 
| Ingredient | Strength | 
|---|---|
| NAPROXEN SODIUM | 220 mg/1 | 
| SPL SET ID: | 3ad98149-0239-4c2b-a3ca-02b26a6b5162 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0363-0168 | All Day Pain Relief | Naproxen Sodium | 
| 0363-0169 | All Day Pain Relief | Naproxen Sodium | 
| 0363-0368 | All Day Pain Relief | Naproxen Sodium | 
| 0363-0938 | all day pain relief | Naproxen Sodium | 
| 0363-6099 | ALL DAY PAIN RELIEF | NAPROXEN SODIUM | 
| 0363-9608 | ALL DAY PAIN RELIEF | NAPROXEN SODIUM | 
| 15127-168 | All Day Pain Relief | Naproxen Sodium | 
| 30142-168 | All Day Pain Relief | Naproxen Sodium | 
| 33992-0169 | All Day Pain Relief | Naproxen Sodium | 
| 36800-256 | All Day Pain Relief | Naproxen Sodium | 
| 37205-744 | All Day Pain Relief | Naproxen Sodium | 
| 37808-068 | All Day Pain Relief | Naproxen Sodium | 
| 37808-259 | All Day Pain Relief | Naproxen Sodium | 
| 37808-339 | all day pain relief | Naproxen sodium | 
| 37808-500 | All Day Pain Relief | Naproxen Sodium | 
| 41163-167 | All Day Pain Relief | Naproxen Sodium | 
| 41163-169 | All Day Pain Relief | Naproxen Sodium | 
| 42254-230 | all day pain relief | Naproxen Sodium | 
| 49781-046 | All Day Pain Relief | Naproxen Sodium | 
| 49781-047 | All Day Pain Relief | Naproxen Sodium | 
| 49781-145 | All Day Pain Relief | Naproxen Sodium | 
| 49781-146 | All Day Pain Relief | Naproxen Sodium | 
| 68210-0030 | ALL DAY PAIN RELIEF | ALL DAY PAIN RELIEF | 
| 69517-109 | All Day Pain Relief | All Day Pain Relief | 
| 70005-008 | All Day Pain Relief | All Day Pain Relief | 
| 49781-101 | All Day Pain Relief | All Day Pain Relief | 
| 55315-168 | All Day Pain Relief | All Day Pain Relief | 
| 55315-256 | All Day Pain Relief | All Day Pain Relief | 
| 55315-255 | All Day Pain Relief | All Day Pain Relief | 
| 55315-169 | All Day Pain Relief | All Day Pain Relief | 
| 55319-417 | All Day Pain Relief | All Day Pain Relief | 
| 55319-604 | All Day Pain Relief | All Day Pain Relief | 
| 55319-174 | All Day Pain Relief | All Day Pain Relief | 
| 59726-169 | All Day Pain Relief | All Day Pain Relief | 
| 59779-172 | All Day Pain Relief | All Day Pain Relief | 
| 59726-023 | All Day Pain Relief | All Day Pain Relief | 
| 59726-168 | All Day Pain Relief | All Day Pain Relief | 
| 59726-256 | All Day Pain Relief | All Day Pain Relief | 
| 63940-174 | All Day Pain Relief | All Day Pain Relief |