Product NDC: | 10237-724 |
Proprietary Name: | Orajel Instant Pain Relief for Severe Toothache |
Non Proprietary Name: | Benzocaine and Menthol |
Active Ingredient(s): | 200; 5 mg/g; mg/g & nbsp; Benzocaine and Menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10237-724 |
Labeler Name: | Church & Dwight Co., Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100721 |
Package NDC: | 10237-724-25 |
Package Description: | 1 TUBE in 1 CARTON (10237-724-25) > 7 g in 1 TUBE |
NDC Code | 10237-724-25 |
Proprietary Name | Orajel Instant Pain Relief for Severe Toothache |
Package Description | 1 TUBE in 1 CARTON (10237-724-25) > 7 g in 1 TUBE |
Product NDC | 10237-724 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine and Menthol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100721 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Church & Dwight Co., Inc. |
Substance Name | BENZOCAINE; MENTHOL |
Strength Number | 200; 5 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |