| 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 |