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Pain Relief - 59779-980-05 - (Acetaminophen)

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Drug Information of Pain Relief

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)

Labeler Information of Pain Relief

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 Information of Pain Relief

Package NDC: 59779-980-05
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (59779-980-05) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of Pain Relief

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

Complete Information of Pain Relief


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