Product NDC: | 49738-184 |
Proprietary Name: | Headache Relief |
Non Proprietary Name: | Acetaminophen, Aspirin, Caffeine |
Active Ingredient(s): | 250; 250; 65 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Aspirin, Caffeine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49738-184 |
Labeler Name: | SMART SENSE (Kmart) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120619 |
Package NDC: | 49738-184-10 |
Package Description: | 1 BOTTLE in 1 BOX (49738-184-10) > 100 TABLET in 1 BOTTLE |
NDC Code | 49738-184-10 |
Proprietary Name | Headache Relief |
Package Description | 1 BOTTLE in 1 BOX (49738-184-10) > 100 TABLET in 1 BOTTLE |
Product NDC | 49738-184 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Aspirin, Caffeine |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120619 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | SMART SENSE (Kmart) |
Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
Strength Number | 250; 250; 65 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |