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Orajel Severe Toothache
Orajel Severe Toothache - 10237-722-45 - (Benzocaine)
Drug Information of Orajel Severe Toothache
| Product NDC: | 10237-722 |
| Proprietary Name: | Orajel Severe Toothache |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | .2 mL/mL & nbsp; Benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Orajel Severe Toothache
| Product NDC: | 10237-722 |
| Labeler Name: | Church & Dwight Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110321 |
Package Information of Orajel Severe Toothache
| Package NDC: | 10237-722-45 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (10237-722-45) > 13.3 mL in 1 BOTTLE, GLASS |
NDC Information of Orajel Severe Toothache
| NDC Code | 10237-722-45 |
| Proprietary Name | Orajel Severe Toothache |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (10237-722-45) > 13.3 mL in 1 BOTTLE, GLASS |
| Product NDC | 10237-722 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110321 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Church & Dwight Co., Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | .2 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
