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Lidocaine Hydrochloride
Lidocaine Hydrochloride - 0924-5000-01 - (Lidocaine Hydrochloride)
Drug Information of Lidocaine Hydrochloride
| Product NDC: | 0924-5000 |
| Proprietary Name: | Lidocaine Hydrochloride |
| Non Proprietary Name: | Lidocaine Hydrochloride |
| Active Ingredient(s): | 20 mg/g & nbsp; Lidocaine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine Hydrochloride
| Product NDC: | 0924-5000 |
| Labeler Name: | Acme United Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130214 |
Package Information of Lidocaine Hydrochloride
| Package NDC: | 0924-5000-01 |
| Package Description: | 6 PACKET in 1 BOX (0924-5000-01) > 3.5 g in 1 PACKET |
NDC Information of Lidocaine Hydrochloride
| NDC Code | 0924-5000-01 |
| Proprietary Name | Lidocaine Hydrochloride |
| Package Description | 6 PACKET in 1 BOX (0924-5000-01) > 3.5 g in 1 PACKET |
| Product NDC | 0924-5000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Lidocaine Hydrochloride |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20130214 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Acme United Corporation |
| Substance Name | LIDOCAINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
