Product NDC: | 10157-9077 |
Proprietary Name: | Ivarest |
Non Proprietary Name: | Zinc Oxide, Benzyl Alcohol, and Diphenhydramine Hydrochloride |
Active Ingredient(s): | 10.5; 2; 14 g/100g; g/100g; g/100g & nbsp; Zinc Oxide, Benzyl Alcohol, and Diphenhydramine Hydrochloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10157-9077 |
Labeler Name: | Blistex Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20071231 |
Package NDC: | 10157-9077-1 |
Package Description: | 1 TUBE in 1 CARTON (10157-9077-1) > 56 g in 1 TUBE |
NDC Code | 10157-9077-1 |
Proprietary Name | Ivarest |
Package Description | 1 TUBE in 1 CARTON (10157-9077-1) > 56 g in 1 TUBE |
Product NDC | 10157-9077 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Zinc Oxide, Benzyl Alcohol, and Diphenhydramine Hydrochloride |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20071231 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Blistex Inc |
Substance Name | BENZYL ALCOHOL; DIPHENHYDRAMINE HYDROCHLORIDE; ZINC OXIDE |
Strength Number | 10.5; 2; 14 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |