| Product NDC: | 41167-4244 | 
| Proprietary Name: | Childrens Allegra Allergy | 
| Non Proprietary Name: | Fexofenadine Hydrochloride | 
| Active Ingredient(s): | 6 mg/mL & nbsp; Fexofenadine Hydrochloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | SUSPENSION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 41167-4244 | 
| Labeler Name: | Chattem, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | NDA201373 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20110303 | 
| Package NDC: | 41167-4244-4 | 
| Package Description: | 1 BOTTLE in 1 CARTON (41167-4244-4) > 120 mL in 1 BOTTLE | 
| NDC Code | 41167-4244-4 | 
| Proprietary Name | Childrens Allegra Allergy | 
| Package Description | 1 BOTTLE in 1 CARTON (41167-4244-4) > 120 mL in 1 BOTTLE | 
| Product NDC | 41167-4244 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Fexofenadine Hydrochloride | 
| Dosage Form Name | SUSPENSION | 
| Route Name | ORAL | 
| Start Marketing Date | 20110303 | 
| Marketing Category Name | NDA | 
| Labeler Name | Chattem, Inc. | 
| Substance Name | FEXOFENADINE HYDROCHLORIDE | 
| Strength Number | 6 | 
| Strength Unit | mg/mL | 
| Pharmaceutical Classes |