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Childrens Mucinex Multi-Symptom Cold
Childrens Mucinex Multi-Symptom Cold - 63824-282-64 - (Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride)
Drug Information of Childrens Mucinex Multi-Symptom Cold
| Product NDC: | 63824-282 |
| Proprietary Name: | Childrens Mucinex Multi-Symptom Cold |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 5; 100; 2.5 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Childrens Mucinex Multi-Symptom Cold
| Product NDC: | 63824-282 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120717 |
Package Information of Childrens Mucinex Multi-Symptom Cold
| Package NDC: | 63824-282-64 |
| Package Description: | 1 BOTTLE in 1 CARTON (63824-282-64) > 118 mL in 1 BOTTLE |
NDC Information of Childrens Mucinex Multi-Symptom Cold
| NDC Code | 63824-282-64 |
| Proprietary Name | Childrens Mucinex Multi-Symptom Cold |
| Package Description | 1 BOTTLE in 1 CARTON (63824-282-64) > 118 mL in 1 BOTTLE |
| Product NDC | 63824-282 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20120717 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 5; 100; 2.5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
