Product NDC: | 11673-572 |
Proprietary Name: | glycerin, phenylephrine hydrochloride, pramoxine, white petrolatum |
Non Proprietary Name: | glycerin, phenylephrine hydrochloride, pramoxine, white petrolatum |
Active Ingredient(s): | .144; .15; .0025; .01 mg/g; mg/g; mg/g; mg/g & nbsp; glycerin, phenylephrine hydrochloride, pramoxine, white petrolatum |
Administration Route(s): | RECTAL; TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11673-572 |
Labeler Name: | Target Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part346 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090401 |
Package NDC: | 11673-572-24 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 BOX (11673-572-24) > 51 g in 1 TUBE, WITH APPLICATOR |
NDC Code | 11673-572-24 |
Proprietary Name | glycerin, phenylephrine hydrochloride, pramoxine, white petrolatum |
Package Description | 1 TUBE, WITH APPLICATOR in 1 BOX (11673-572-24) > 51 g in 1 TUBE, WITH APPLICATOR |
Product NDC | 11673-572 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | glycerin, phenylephrine hydrochloride, pramoxine, white petrolatum |
Dosage Form Name | CREAM |
Route Name | RECTAL; TOPICAL |
Start Marketing Date | 20090401 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Target Corporation |
Substance Name | GLYCERIN; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE |
Strength Number | .144; .15; .0025; .01 |
Strength Unit | mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes |