Product NDC: | 10237-705 |
Proprietary Name: | Orajel for Toothache |
Non Proprietary Name: | Benzocaine |
Active Ingredient(s): | .2 mL/mL & nbsp; Benzocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SWAB |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10237-705 |
Labeler Name: | Church & Dwight Co., Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100811 |
Package NDC: | 10237-705-12 |
Package Description: | 12 APPLICATOR in 1 CARTON (10237-705-12) > 1.8 mL in 1 APPLICATOR |
NDC Code | 10237-705-12 |
Proprietary Name | Orajel for Toothache |
Package Description | 12 APPLICATOR in 1 CARTON (10237-705-12) > 1.8 mL in 1 APPLICATOR |
Product NDC | 10237-705 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine |
Dosage Form Name | SWAB |
Route Name | TOPICAL |
Start Marketing Date | 20100811 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Church & Dwight Co., Inc. |
Substance Name | BENZOCAINE |
Strength Number | .2 |
Strength Unit | mL/mL |
Pharmaceutical Classes |