| Product NDC: | 63029-900 | 
| Proprietary Name: | PediaCare Infants | 
| Non Proprietary Name: | Ibuprofen | 
| Active Ingredient(s): | 50 mg/1.25mL & nbsp; Ibuprofen | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 63029-900 | 
| Labeler Name: | Medtech Products Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part343 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20111015 | 
| Package NDC: | 63029-900-01 | 
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (63029-900-01) > 30 mL in 1 BOTTLE, WITH APPLICATOR | 
| NDC Code | 63029-900-01 | 
| Proprietary Name | PediaCare Infants | 
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (63029-900-01) > 30 mL in 1 BOTTLE, WITH APPLICATOR | 
| Product NDC | 63029-900 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Ibuprofen | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20111015 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Medtech Products Inc. | 
| Substance Name | IBUPROFEN | 
| Strength Number | 50 | 
| Strength Unit | mg/1.25mL | 
| Pharmaceutical Classes |