Home
>
National Drug Code (NDC)
>
Pain Relief
Pain Relief - 56062-161-10 - (Acetaminophen)
Drug Information of Pain Relief
| Product NDC: | 56062-161 |
| Proprietary Name: | Pain Relief |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 160 mg/5mL & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pain Relief
| Product NDC: | 56062-161 |
| Labeler Name: | Publix Super Markets Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111129 |
Package Information of Pain Relief
| Package NDC: | 56062-161-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (56062-161-10) > 30 mL in 1 BOTTLE |
NDC Information of Pain Relief
| NDC Code | 56062-161-10 |
| Proprietary Name | Pain Relief |
| Package Description | 1 BOTTLE in 1 CARTON (56062-161-10) > 30 mL in 1 BOTTLE |
| Product NDC | 56062-161 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20111129 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Publix Super Markets Inc |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 160 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
