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CounterAct
CounterAct - 54473-139-36 - (Acetaminophen, Diphenhydramine HCI, Phenylephrine HCI)
Drug Information of CounterAct
| Product NDC: | 54473-139 |
| Proprietary Name: | CounterAct |
| Non Proprietary Name: | Acetaminophen, Diphenhydramine HCI, Phenylephrine HCI |
| Active Ingredient(s): | 325; 25; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine HCI, Phenylephrine HCI |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CounterAct
| Product NDC: | 54473-139 |
| Labeler Name: | Melaleuca, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091021 |
Package Information of CounterAct
| Package NDC: | 54473-139-36 |
| Package Description: | 3 BLISTER PACK in 1 BOX (54473-139-36) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of CounterAct
| NDC Code | 54473-139-36 |
| Proprietary Name | CounterAct |
| Package Description | 3 BLISTER PACK in 1 BOX (54473-139-36) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 54473-139 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Diphenhydramine HCI, Phenylephrine HCI |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091021 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Melaleuca, Inc. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 25; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
