Product NDC: | 10237-726 |
Proprietary Name: | Orajel for Codl Sores Relief and Concealer |
Non Proprietary Name: | Allantoin Benzocaine Camphor |
Active Ingredient(s): | 5; 200; 30; 20; 10; 640 mg/g; mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; Allantoin Benzocaine Camphor |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10237-726 |
Labeler Name: | Church & Dwight Co., Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100719 |
Package NDC: | 10237-726-05 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 BLISTER PACK (10237-726-05) > 1.4 g in 1 TUBE, WITH APPLICATOR |
NDC Code | 10237-726-05 |
Proprietary Name | Orajel for Codl Sores Relief and Concealer |
Package Description | 1 TUBE, WITH APPLICATOR in 1 BLISTER PACK (10237-726-05) > 1.4 g in 1 TUBE, WITH APPLICATOR |
Product NDC | 10237-726 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Allantoin Benzocaine Camphor |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100719 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Church & Dwight Co., Inc. |
Substance Name | ALLANTOIN; BENZOCAINE; CAMPHOR (NATURAL); DIMETHICONE; MENTHOL; PETROLATUM |
Strength Number | 5; 200; 30; 20; 10; 640 |
Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes |