Product NDC: | 11822-0012 |
Proprietary Name: | Junior Pain Relief |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 160 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-0012 |
Labeler Name: | Rite Aid |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20050225 |
Package NDC: | 11822-0012-8 |
Package Description: | 1 BLISTER PACK in 1 CARTON (11822-0012-8) > 24 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Code | 11822-0012-8 |
Proprietary Name | Junior Pain Relief |
Package Description | 1 BLISTER PACK in 1 CARTON (11822-0012-8) > 24 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
Product NDC | 11822-0012 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
Route Name | ORAL |
Start Marketing Date | 20050225 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Rite Aid |
Substance Name | ACETAMINOPHEN |
Strength Number | 160 |
Strength Unit | mg/1 |
Pharmaceutical Classes |