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Rx Act Pain Relief
Rx Act Pain Relief - 37808-046-83 - (Acetaminophen)
Drug Information of Rx Act Pain Relief
| Product NDC: | 37808-046 |
| Proprietary Name: | Rx Act Pain Relief |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rx Act Pain Relief
| Product NDC: | 37808-046 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100201 |
Package Information of Rx Act Pain Relief
| Package NDC: | 37808-046-83 |
| Package Description: | 225 TABLET, COATED in 1 BOTTLE (37808-046-83) |
NDC Information of Rx Act Pain Relief
| NDC Code | 37808-046-83 |
| Proprietary Name | Rx Act Pain Relief |
| Package Description | 225 TABLET, COATED in 1 BOTTLE (37808-046-83) |
| Product NDC | 37808-046 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H E B |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
