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Orajel
Orajel - 10237-743-42 - (Sodium Fluoride)
Drug Information of Orajel
| Product NDC: | 10237-743 |
| Proprietary Name: | Orajel |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 2.4 mg/g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Orajel
| Product NDC: | 10237-743 |
| Labeler Name: | Church & Dwight Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130201 |
Package Information of Orajel
| Package NDC: | 10237-743-42 |
| Package Description: | 1 TUBE in 1 CARTON (10237-743-42) > 119 g in 1 TUBE |
NDC Information of Orajel
| NDC Code | 10237-743-42 |
| Proprietary Name | Orajel |
| Package Description | 1 TUBE in 1 CARTON (10237-743-42) > 119 g in 1 TUBE |
| Product NDC | 10237-743 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | GEL, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20130201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Church & Dwight Co., Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2.4 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
