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Blistex
Blistex - 10157-9848-2 - (Dimethicone, Octinoxate, Oxybenzone, and Lanolin)
Drug Information of Blistex
| Product NDC: | 10157-9848 |
| Proprietary Name: | Blistex |
| Non Proprietary Name: | Dimethicone, Octinoxate, Oxybenzone, and Lanolin |
| Active Ingredient(s): | & nbsp; Dimethicone, Octinoxate, Oxybenzone, and Lanolin |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Blistex
| Product NDC: | 10157-9848 |
| Labeler Name: | Blistex Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110613 |
Package Information of Blistex
| Package NDC: | 10157-9848-2 |
| Package Description: | 1 KIT in 1 PACKAGE (10157-9848-2) * 5.67 g in 1 JAR * 5.67 g in 1 JAR |
NDC Information of Blistex
| NDC Code | 10157-9848-2 |
| Proprietary Name | Blistex |
| Package Description | 1 KIT in 1 PACKAGE (10157-9848-2) * 5.67 g in 1 JAR * 5.67 g in 1 JAR |
| Product NDC | 10157-9848 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dimethicone, Octinoxate, Oxybenzone, and Lanolin |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110613 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Blistex Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
