Product NDC: | 52183-325 |
Proprietary Name: | PediaCare Childrens Fever Reducer Pain Reliever Dye Free |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 160 mg/5mL & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52183-325 |
Labeler Name: | Blacksmith Brands, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100802 |
Package NDC: | 52183-325-04 |
Package Description: | 1 BOTTLE in 1 BOX (52183-325-04) > 118 mL in 1 BOTTLE |
NDC Code | 52183-325-04 |
Proprietary Name | PediaCare Childrens Fever Reducer Pain Reliever Dye Free |
Package Description | 1 BOTTLE in 1 BOX (52183-325-04) > 118 mL in 1 BOTTLE |
Product NDC | 52183-325 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20100802 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Blacksmith Brands, Inc. |
Substance Name | ACETAMINOPHEN |
Strength Number | 160 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |