NDC 69313-633

LidoFLEX Elbow, Single Pouch

Lidoflex Elbow

LidoFLEX Elbow, Single Pouch 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: 69313-633_444511c6-ef0b-2d22-e054-00144ff8d46c
• NDC: 69313-633
• Product Type: Human Otc Drug
• Proprietary Name: LidoFLEX Elbow, Single Pouch
• Generic Name: Lidoflex Elbow
• 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: 22 mg/.24mg
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 69313-633-01

21.5 mg in 1 POUCH (69313-633-01)

• Marketing Start Date: 2014-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69313-633-01 [69313063301]

LidoFLEX Elbow, Single Pouch PATCH

• 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

NDC 69313-633-20 [69313063320]

LidoFLEX Elbow, Single Pouch PATCH

• 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

NDC 69313-633-05 [69313063305]

LidoFLEX Elbow, Single Pouch PATCH

• 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

Drug Details

Active Ingredients

Ingredient	Strength
LIDOCAINE	21.5 mg/.24mg

OpenFDA Data

• SPL SET ID: 06041bf8-07d7-3a70-e054-00144ff8d46c
• Manufacturer:
  • NAIMCO, INC. DBA RICHMAR, INC.
• UNII:
  • 98PI200987
• UPC Code:
  • 0369313632057
  • 0369313637052
  • 0369313634051
  • 0369313633054
  • 0369313635058
  • 0369313636055