NDC 70512-011

Lenza Pro

Lidocaine/menthol Patch

Lenza Pro is a Topical Patch in the Human Otc Drug category. It is labeled and distributed by Kbs Solutions. The primary component is Lidocaine; Menthol.

• Product ID: 70512-011_6d8c4b22-3e75-d3bd-e053-2991aa0a793d
• NDC: 70512-011
• Product Type: Human Otc Drug
• Proprietary Name: Lenza Pro
• Generic Name: Lidocaine/menthol Patch
• Dosage Form: Patch
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-02-08
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Labeler Name: KBS Solutions
• Substance Name: LIDOCAINE; MENTHOL
• Active Ingredient Strength: 40 mg/g; mg/g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 70512-011-15

3 POUCH in 1 BOX (70512-011-15) > 1 g in 1 POUCH

• Marketing Start Date: 2018-02-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70512-011-15 [70512001115]

Lenza Pro PATCH

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-02-08

Drug Details

Active Ingredients

Ingredient	Strength
LIDOCAINE	40 mg/g

OpenFDA Data

• SPL SET ID: 661ef396-0b38-6e1a-e053-2a91aa0a8352
• Manufacturer:
  • KBS Solutions
• UNII:
  • 98PI200987
  • L7T10EIP3A
• RxNorm Concept Unique ID - RxCUI:
  • 1428948
• UPC Code:
  • 0070512011153