Product NDC: | 63029-639 |
Proprietary Name: | Goodys Headache Relief Shot |
Non Proprietary Name: | Acetaminophen and Caffeine |
Active Ingredient(s): | 1000; 65 mg/60mL; mg/60mL & nbsp; Acetaminophen and Caffeine |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63029-639 |
Labeler Name: | Medtech Products Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130211 |
Package NDC: | 63029-639-01 |
Package Description: | 2 BOTTLE, UNIT-DOSE in 1 DOSE PACK (63029-639-01) > 60 mL in 1 BOTTLE, UNIT-DOSE |
NDC Code | 63029-639-01 |
Proprietary Name | Goodys Headache Relief Shot |
Package Description | 2 BOTTLE, UNIT-DOSE in 1 DOSE PACK (63029-639-01) > 60 mL in 1 BOTTLE, UNIT-DOSE |
Product NDC | 63029-639 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen and Caffeine |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20130211 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medtech Products Inc. |
Substance Name | ACETAMINOPHEN; CAFFEINE |
Strength Number | 1000; 65 |
Strength Unit | mg/60mL; mg/60mL |
Pharmaceutical Classes |