Product NDC: | 51596-008 |
Proprietary Name: | Ache and Pain Relief to Go |
Non Proprietary Name: | aspirin and caffeine |
Active Ingredient(s): | 650; 60 mg/1; mg/1 & nbsp; aspirin and caffeine |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51596-008 |
Labeler Name: | Breakthrough Products Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121001 |
Package NDC: | 51596-008-01 |
Package Description: | 1 POWDER in 1 POUCH (51596-008-01) |
NDC Code | 51596-008-01 |
Proprietary Name | Ache and Pain Relief to Go |
Package Description | 1 POWDER in 1 POUCH (51596-008-01) |
Product NDC | 51596-008 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | aspirin and caffeine |
Dosage Form Name | POWDER |
Route Name | ORAL |
Start Marketing Date | 20121001 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Breakthrough Products Inc. |
Substance Name | ASPIRIN; CAFFEINE |
Strength Number | 650; 60 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |