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Mucinex Sinus-Max Day Night
Mucinex Sinus-Max Day Night - 63824-202-20 - (Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride, and Diphenhydramine Hydrochloride)
Drug Information of Mucinex Sinus-Max Day Night
| Product NDC: | 63824-202 |
| Proprietary Name: | Mucinex Sinus-Max Day Night |
| Non Proprietary Name: | Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride, and Diphenhydramine Hydrochloride |
| Active Ingredient(s): | & nbsp; Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride, and Diphenhydramine Hydrochloride |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucinex Sinus-Max Day Night
| Product NDC: | 63824-202 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120910 |
Package Information of Mucinex Sinus-Max Day Night
| Package NDC: | 63824-202-20 |
| Package Description: | 1 KIT in 1 CARTON (63824-202-20) * 5 TABLET in 1 BLISTER PACK * 5 TABLET in 1 BLISTER PACK |
NDC Information of Mucinex Sinus-Max Day Night
| NDC Code | 63824-202-20 |
| Proprietary Name | Mucinex Sinus-Max Day Night |
| Package Description | 1 KIT in 1 CARTON (63824-202-20) * 5 TABLET in 1 BLISTER PACK * 5 TABLET in 1 BLISTER PACK |
| Product NDC | 63824-202 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride, and Diphenhydramine Hydrochloride |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120910 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
