 
                        | Product NDC: | 63824-127 | 
| Proprietary Name: | Mucinex Sinus-Max | 
| Non Proprietary Name: | Oxymetazoline Hydrochloride | 
| Active Ingredient(s): | .05 mg/100mL & nbsp; Oxymetazoline Hydrochloride | 
| Administration Route(s): | NASAL | 
| Dosage Form(s): | SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 63824-127 | 
| Labeler Name: | Reckitt Benckiser LLC | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20120901 | 
| Package NDC: | 63824-127-75 | 
| Package Description: | 1 BOTTLE in 1 CARTON (63824-127-75) > 22 mL in 1 BOTTLE | 
| NDC Code | 63824-127-75 | 
| Proprietary Name | Mucinex Sinus-Max | 
| Package Description | 1 BOTTLE in 1 CARTON (63824-127-75) > 22 mL in 1 BOTTLE | 
| Product NDC | 63824-127 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Oxymetazoline Hydrochloride | 
| Dosage Form Name | SOLUTION | 
| Route Name | NASAL | 
| Start Marketing Date | 20120901 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Reckitt Benckiser LLC | 
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE | 
| Strength Number | .05 | 
| Strength Unit | mg/100mL | 
| Pharmaceutical Classes |