| 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 |