| 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 |