| Product NDC: | 59779-980 | 
| Proprietary Name: | Pain Relief | 
| Non Proprietary Name: | Acetaminophen | 
| Active Ingredient(s): | 80 mg/.8mL & nbsp; Acetaminophen | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | SUSPENSION/ DROPS | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-980 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part343 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20100825 | 
| Package NDC: | 59779-980-05 | 
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (59779-980-05) > 15 mL in 1 BOTTLE, DROPPER | 
| NDC Code | 59779-980-05 | 
| Proprietary Name | Pain Relief | 
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (59779-980-05) > 15 mL in 1 BOTTLE, DROPPER | 
| Product NDC | 59779-980 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen | 
| Dosage Form Name | SUSPENSION/ DROPS | 
| Route Name | ORAL | 
| Start Marketing Date | 20100825 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | ACETAMINOPHEN | 
| Strength Number | 80 | 
| Strength Unit | mg/.8mL | 
| Pharmaceutical Classes |