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Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu
Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu - 63824-551-30 - (Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride)
Drug Information of Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu
| Product NDC: | 63824-551 |
| Proprietary Name: | Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride |
| Active Ingredient(s): | & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu
| Product NDC: | 63824-551 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130501 |
Package Information of Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu
| Package NDC: | 63824-551-30 |
| Package Description: | 1 KIT in 1 CARTON (63824-551-30) * 10 TABLET, COATED in 1 BLISTER PACK * 10 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu
| NDC Code | 63824-551-30 |
| Proprietary Name | Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu |
| Package Description | 1 KIT in 1 CARTON (63824-551-30) * 10 TABLET, COATED in 1 BLISTER PACK * 10 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 63824-551 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
