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rx act pain relief - 37808-008-10 - (Acetaminophen)

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Drug Information of rx act pain relief

Product NDC: 37808-008
Proprietary Name: rx act 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 rx act pain relief

Product NDC: 37808-008
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19910615

Package Information of rx act pain relief

Package NDC: 37808-008-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (37808-008-10) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of rx act pain relief

NDC Code 37808-008-10
Proprietary Name rx act pain relief
Package Description 1 BOTTLE, DROPPER in 1 CARTON (37808-008-10) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 37808-008
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUSPENSION/ DROPS
Route Name ORAL
Start Marketing Date 19910615
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name H E B
Substance Name ACETAMINOPHEN
Strength Number 80
Strength Unit mg/.8mL
Pharmaceutical Classes

Complete Information of rx act pain relief


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