| Product NDC: | 10157-9800 |
| Proprietary Name: | Blistex |
| Non Proprietary Name: | Dimethicone, Octinoxate, and Oxybenzone |
| Active Ingredient(s): | 1; 7.5; 2.5 g/100g; g/100g; g/100g & nbsp; Dimethicone, Octinoxate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10157-9800 |
| Labeler Name: | Blistex Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101101 |
| Package NDC: | 10157-9800-1 |
| Package Description: | 4.25 g in 1 CYLINDER (10157-9800-1) |
| NDC Code | 10157-9800-1 |
| Proprietary Name | Blistex |
| Package Description | 4.25 g in 1 CYLINDER (10157-9800-1) |
| Product NDC | 10157-9800 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dimethicone, Octinoxate, and Oxybenzone |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20101101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Blistex Inc |
| Substance Name | DIMETHICONE; OCTINOXATE; OXYBENZONE |
| Strength Number | 1; 7.5; 2.5 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |