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CounterAct
CounterAct - 54473-182-50 - (Acetaminophen and Diphenhydramine)
Drug Information of CounterAct
| Product NDC: | 54473-182 |
| Proprietary Name: | CounterAct |
| Non Proprietary Name: | Acetaminophen and Diphenhydramine |
| Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; Acetaminophen and Diphenhydramine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CounterAct
| Product NDC: | 54473-182 |
| Labeler Name: | Melaleuca, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110401 |
Package Information of CounterAct
| Package NDC: | 54473-182-50 |
| Package Description: | 1 BOTTLE in 1 BOX (54473-182-50) > 50 TABLET in 1 BOTTLE |
NDC Information of CounterAct
| NDC Code | 54473-182-50 |
| Proprietary Name | CounterAct |
| Package Description | 1 BOTTLE in 1 BOX (54473-182-50) > 50 TABLET in 1 BOTTLE |
| Product NDC | 54473-182 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Diphenhydramine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Melaleuca, Inc. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
