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Oral Analgesic
Oral Analgesic - 41250-706-21 - (Benzocaine and Menthol)
Drug Information of Oral Analgesic
| Product NDC: | 41250-706 |
| Proprietary Name: | Oral Analgesic |
| Non Proprietary Name: | Benzocaine and Menthol |
| Active Ingredient(s): | 200; 2.5 mg/g; mg/g & nbsp; Benzocaine and Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oral Analgesic
| Product NDC: | 41250-706 |
| Labeler Name: | Meijer Distribution Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100513 |
Package Information of Oral Analgesic
| Package NDC: | 41250-706-21 |
| Package Description: | 1 TUBE in 1 CARTON (41250-706-21) > 6 g in 1 TUBE |
NDC Information of Oral Analgesic
| NDC Code | 41250-706-21 |
| Proprietary Name | Oral Analgesic |
| Package Description | 1 TUBE in 1 CARTON (41250-706-21) > 6 g in 1 TUBE |
| Product NDC | 41250-706 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine and Menthol |
| Dosage Form Name | PASTE |
| Route Name | TOPICAL |
| Start Marketing Date | 20100513 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Meijer Distribution Inc. |
| Substance Name | BENZOCAINE; MENTHOL |
| Strength Number | 200; 2.5 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
