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pain relief - 56062-175-26 - (Acetaminophen)

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Drug Information of pain relief

Product NDC: 56062-175
Proprietary Name: pain relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 160    mg/5mL & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of pain relief

Product NDC: 56062-175
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20030828

Package Information of pain relief

Package NDC: 56062-175-26
Package Description: 1 BOTTLE in 1 CARTON (56062-175-26) > 118 mL in 1 BOTTLE

NDC Information of pain relief

NDC Code 56062-175-26
Proprietary Name pain relief
Package Description 1 BOTTLE in 1 CARTON (56062-175-26) > 118 mL in 1 BOTTLE
Product NDC 56062-175
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20030828
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

Complete Information of pain relief


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