LidoFLEX is a Topical Patch in the Human Otc Drug category. It is labeled and distributed by Naimco, Inc. Dba Richmar, Inc.. The primary component is Lidocaine.
Product ID | 69313-634_444511c6-ef0b-2d22-e054-00144ff8d46c |
NDC | 69313-634 |
Product Type | Human Otc Drug |
Proprietary Name | LidoFLEX |
Generic Name | Lidoflex Heel |
Dosage Form | Patch |
Route of Administration | TOPICAL |
Marketing Start Date | 2014-09-01 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part348 |
Labeler Name | NAIMCO, INC. DBA RICHMAR, INC. |
Substance Name | LIDOCAINE |
Active Ingredient Strength | 23 mg/.24mg |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2014-10-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part348 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-10-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part348 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-10-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part348 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-10-01 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
LIDOCAINE | 22.7 mg/.24mg |
SPL SET ID: | 06041bf8-07d7-3a70-e054-00144ff8d46c |
Manufacturer | |
UNII | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
69313-632 | LidoFLEX | LidoFLEX Single Pouch, Back |
69313-633 | LidoFLEX | LidoFLEX Elbow |
69313-634 | LidoFLEX | LidoFLEX Heel |
69313-635 | LidoFLEX | LidoFLEX Single Pouch, Knee |
69313-636 | LidoFLEX | LidoFLEX Shoulder |
69313-637 | LidoFLEX | LidoFLEX Flex Strip Double |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LIDOFLEX 86420555 4869342 Live/Registered |
NAIMCO, INC. 2014-10-10 |