NDC 52183-225

Ludens Dual Relief

Pectin And Menthol

Ludens Dual Relief is a Oral Lozenge in the Human Otc Drug category. It is labeled and distributed by Prestige Brands Holdings, Inc.. The primary component is Pectin; Menthol.

• Product ID: 52183-225_6c75b202-112a-4d70-b1dc-8675d7a8090e
• NDC: 52183-225
• Product Type: Human Otc Drug
• Proprietary Name: Ludens Dual Relief
• Generic Name: Pectin And Menthol
• Dosage Form: Lozenge
• Route of Administration: ORAL
• Marketing Start Date: 2018-06-15
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Prestige Brands Holdings, Inc.
• Substance Name: PECTIN; MENTHOL
• Active Ingredient Strength: 3 mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 52183-225-25

25 LOZENGE in 1 BAG (52183-225-25)

• Marketing Start Date: 2018-06-15
• Marketing End Date: 2023-09-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 52183-225-25 [52183022525]

Ludens Dual Relief LOZENGE

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-06-15
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
PECTIN	2.8 mg/1

OpenFDA Data

• SPL SET ID: 4655aa98-4532-4a70-9ae6-693f4c312b41
• Manufacturer:
  • Prestige Brands Holdings, Inc.
• UNII:
  • L7T10EIP3A
  • 89NA02M4RX
• RxNorm Concept Unique ID - RxCUI:
  • 2056069
  • 2056063

NDC Crossover Matching brand name "Ludens Dual Relief" or generic name "Pectin And Menthol"

NDC	Brand Name	Generic Name
52183-225	Ludens	pectin and menthol
52183-227	Ludens	pectin and menthol