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Cutiecaine
Cutiecaine - 51350-111-02 - (Topical Lidocaine (5% w/w))
Drug Information of Cutiecaine
| Product NDC: | 51350-111 |
| Proprietary Name: | Cutiecaine |
| Non Proprietary Name: | Topical Lidocaine (5% w/w) |
| Active Ingredient(s): | 50 mg/g & nbsp; Topical Lidocaine (5% w/w) |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cutiecaine
| Product NDC: | 51350-111 |
| Labeler Name: | Transdermal Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111115 |
Package Information of Cutiecaine
| Package NDC: | 51350-111-02 |
| Package Description: | 1 TUBE in 1 CARTON (51350-111-02) > 15 g in 1 TUBE (51350-111-01) |
NDC Information of Cutiecaine
| NDC Code | 51350-111-02 |
| Proprietary Name | Cutiecaine |
| Package Description | 1 TUBE in 1 CARTON (51350-111-02) > 15 g in 1 TUBE (51350-111-01) |
| Product NDC | 51350-111 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Topical Lidocaine (5% w/w) |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111115 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Transdermal Corp |
| Substance Name | LIDOCAINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
