NDC 43742-0562

CHOLESTEROL

Cholesterinum

CHOLESTEROL is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Cholesterol.

• Product ID: 43742-0562_0efaaf88-f7f4-4fa8-8fff-53cf6ef3ea2b
• NDC: 43742-0562
• Product Type: Human Otc Drug
• Proprietary Name: CHOLESTEROL
• Generic Name: Cholesterinum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2015-01-19
• Marketing End Date: 2023-06-06
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: CHOLESTEROL
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0562-1

30 mL in 1 BOTTLE, DROPPER (43742-0562-1)

• Marketing Start Date: 2016-04-21
• Marketing End Date: 2023-06-06
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0562-1 [43742056201]

CHOLESTEROL LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-04-21
• Marketing End Date: 2023-06-06

Drug Details

Active Ingredients

Ingredient	Strength
CHOLESTEROL	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 06d72b32-f4cc-4c8f-a449-91146bbc41e1
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 97C5T2UQ7J

NDC Crossover Matching brand name "CHOLESTEROL" or generic name "Cholesterinum"

NDC	Brand Name	Generic Name
43742-0562	CHOLESTEROL	Cholesterinum
43742-1272	Cholesterol	Cholesterinum
63083-1551	Cholesterol	Cholesterol
0220-1334	Cholesterinum	CHOLESTEROL
0220-1335	Cholesterinum	CHOLESTEROL
0220-1339	Cholesterinum	CHOLESTEROL
0220-1341	Cholesterinum	CHOLESTEROL
15631-0132	CHOLESTERINUM	CHOLESTERINUM
68428-315	Cholesterinum	CHOLESTEROL
71919-194	Cholesterinum	CHOLESTEROL