NDC 68788-7503

NuLido

Lidocaine Hydrocloride 4%

NuLido is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is Lidocaine; Menthol, Unspecified Form.

• Product ID: 68788-7503_50f78db6-ab2b-47dc-b1d8-690c9408438b
• NDC: 68788-7503
• Product Type: Human Otc Drug
• Proprietary Name: NuLido
• Generic Name: Lidocaine Hydrocloride 4%
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2017-10-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Labeler Name: Preferred Pharmaceuticals, Inc.
• Substance Name: LIDOCAINE; MENTHOL, UNSPECIFIED FORM
• Active Ingredient Strength: 4 mg/mL; mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 68788-7503-1

120 mL in 1 TUBE (68788-7503-1)

• Marketing Start Date: 2019-12-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68788-7503-1 [68788750301]

NuLido GEL

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-12-27

Drug Details

Active Ingredients

Ingredient	Strength
LIDOCAINE	4 mg/mL

OpenFDA Data

• SPL SET ID: 50f78db6-ab2b-47dc-b1d8-690c9408438b
• Manufacturer:
  • Preferred Pharmaceuticals, Inc.
• UNII:
  • 98PI200987
  • L7T10EIP3A
• RxNorm Concept Unique ID - RxCUI:
  • 1804176

NDC Crossover Matching brand name "NuLido" or generic name "Lidocaine Hydrocloride 4%"

NDC	Brand Name	Generic Name
53149-2100	NuLido	Lidocaine Hydrocloride 4%
68788-7503	NuLido	Lidocaine Hydrocloride 4%
76420-140	NuLido	Lidocaine Hydrocloride 4%