NDC 63736-012

Kondremul

Kondremul

Kondremul is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Insight Pharmaceuticals. The primary component is Mineral Oil.

• Product ID: 63736-012_856ae077-f23b-40bf-9a06-09e6f0d56d19
• NDC: 63736-012
• Product Type: Human Otc Drug
• Proprietary Name: Kondremul
• Generic Name: Kondremul
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2009-06-05
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part334
• Labeler Name: Insight Pharmaceuticals
• Substance Name: MINERAL OIL
• Active Ingredient Strength: 3 mL/5mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 63736-012-16

480 mL in 1 BOTTLE (63736-012-16)

• Marketing Start Date: 2009-06-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63736-012-16 [63736001216]

Kondremul LIQUID

• Marketing Category: OTC monograph final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-06-05
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
MINERAL OIL	2.5 mL/5mL

OpenFDA Data

• SPL SET ID: 116e0ea5-c649-47ef-a9d2-fc683aed229c
• Manufacturer:
  • Insight Pharmaceuticals
• UNII:
  • T5L8T28FGP
• RxNorm Concept Unique ID - RxCUI:
  • 1489229

NDC Crossover Matching brand name "Kondremul" or generic name "Kondremul"

NDC	Brand Name	Generic Name
63736-012	Kondremul	Kondremul
63736-042	Kondremul	Mineral Oil