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Dr. Numb
Dr. Numb - 52512-130-30 - (Lidocaine)
Drug Information of Dr. Numb
| Product NDC: | 52512-130 |
| Proprietary Name: | Dr. Numb |
| Non Proprietary Name: | Lidocaine |
| Active Ingredient(s): | 5 g/100g & nbsp; Lidocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dr. Numb
| Product NDC: | 52512-130 |
| Labeler Name: | Ei Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121115 |
Package Information of Dr. Numb
| Package NDC: | 52512-130-30 |
| Package Description: | 1 TUBE in 1 PACKAGE (52512-130-30) > 30 g in 1 TUBE |
NDC Information of Dr. Numb
| NDC Code | 52512-130-30 |
| Proprietary Name | Dr. Numb |
| Package Description | 1 TUBE in 1 PACKAGE (52512-130-30) > 30 g in 1 TUBE |
| Product NDC | 52512-130 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Lidocaine |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121115 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ei Inc. |
| Substance Name | LIDOCAINE |
| Strength Number | 5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
