Product NDC: | 10237-738 |
Proprietary Name: | Orajel Nighttime Instant Relief for Teething Pain |
Non Proprietary Name: | Benzocaine |
Active Ingredient(s): | 100 mg/g & nbsp; Benzocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10237-738 |
Labeler Name: | Church & Dwight Co., Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100618 |
Package NDC: | 10237-738-19 |
Package Description: | 1 CARTON in 1 CARTON (10237-738-19) > 1 TUBE in 1 CARTON (10237-738-18) > 5.1 g in 1 TUBE |
NDC Code | 10237-738-19 |
Proprietary Name | Orajel Nighttime Instant Relief for Teething Pain |
Package Description | 1 CARTON in 1 CARTON (10237-738-19) > 1 TUBE in 1 CARTON (10237-738-18) > 5.1 g in 1 TUBE |
Product NDC | 10237-738 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100618 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Church & Dwight Co., Inc. |
Substance Name | BENZOCAINE |
Strength Number | 100 |
Strength Unit | mg/g |
Pharmaceutical Classes |