Product NDC: | 53329-088 |
Proprietary Name: | Anorectal |
Non Proprietary Name: | zinc oxide, petrolatum |
Active Ingredient(s): | 800; 200 mg/g; mg/g & nbsp; zinc oxide, petrolatum |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53329-088 |
Labeler Name: | Medline Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part346 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100301 |
Package NDC: | 53329-088-14 |
Package Description: | 1 TUBE in 1 BOX (53329-088-14) > 56.6 g in 1 TUBE |
NDC Code | 53329-088-14 |
Proprietary Name | Anorectal |
Package Description | 1 TUBE in 1 BOX (53329-088-14) > 56.6 g in 1 TUBE |
Product NDC | 53329-088 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | zinc oxide, petrolatum |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medline Industries, Inc. |
Substance Name | PETROLATUM; ZINC OXIDE |
Strength Number | 800; 200 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |