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Orajel Instant Pain Relief
Orajel Instant Pain Relief - 10237-708-18 - (Benzocaine)
Drug Information of Orajel Instant Pain Relief
| Product NDC: | 10237-708 |
| Proprietary Name: | Orajel Instant Pain Relief |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | .4; 200; 1 mg/g; mg/g; mg/g & nbsp; Benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Orajel Instant Pain Relief
| Product NDC: | 10237-708 |
| Labeler Name: | Church & Dwight Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100611 |
Package Information of Orajel Instant Pain Relief
| Package NDC: | 10237-708-18 |
| Package Description: | 1 TUBE in 1 CARTON (10237-708-18) > 5.1 g in 1 TUBE |
NDC Information of Orajel Instant Pain Relief
| NDC Code | 10237-708-18 |
| Proprietary Name | Orajel Instant Pain Relief |
| Package Description | 1 TUBE in 1 CARTON (10237-708-18) > 5.1 g in 1 TUBE |
| Product NDC | 10237-708 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100611 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Church & Dwight Co., Inc. |
| Substance Name | BENZALKONIUM CHLORIDE; BENZOCAINE; ZINC CHLORIDE |
| Strength Number | .4; 200; 1 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
