Product NDC: | 0573-2871 |
Proprietary Name: | PREPARATION H |
Non Proprietary Name: | mineral oil, petrolatum, phenylephrine HCl |
Active Ingredient(s): | 140; 749; 2.5 mg/g; mg/g; mg/g & nbsp; mineral oil, petrolatum, phenylephrine HCl |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0573-2871 |
Labeler Name: | Pfizer Consumer Healthcare |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part346 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20040301 |
Package NDC: | 0573-2871-20 |
Package Description: | 1 TUBE in 1 CARTON (0573-2871-20) > 57 g in 1 TUBE |
NDC Code | 0573-2871-20 |
Proprietary Name | PREPARATION H |
Package Description | 1 TUBE in 1 CARTON (0573-2871-20) > 57 g in 1 TUBE |
Product NDC | 0573-2871 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | mineral oil, petrolatum, phenylephrine HCl |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20040301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Pfizer Consumer Healthcare |
Substance Name | MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 140; 749; 2.5 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes |