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Derma Numb
Derma Numb - 53200-001-04 - (Lidocaine)
Drug Information of Derma Numb
| Product NDC: | 53200-001 |
| Proprietary Name: | Derma Numb |
| Non Proprietary Name: | Lidocaine |
| Active Ingredient(s): | 40 mg/g & nbsp; Lidocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Derma Numb
| Product NDC: | 53200-001 |
| Labeler Name: | Atlas Tat Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120715 |
Package Information of Derma Numb
| Package NDC: | 53200-001-04 |
| Package Description: | 113.4 g in 1 BOTTLE, SPRAY (53200-001-04) |
NDC Information of Derma Numb
| NDC Code | 53200-001-04 |
| Proprietary Name | Derma Numb |
| Package Description | 113.4 g in 1 BOTTLE, SPRAY (53200-001-04) |
| Product NDC | 53200-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Lidocaine |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20120715 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Atlas Tat Inc. |
| Substance Name | LIDOCAINE |
| Strength Number | 40 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
