NDC 43742-1272

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: 43742-1272_e2c33fb3-c706-4a92-a4b5-175968f4122e
• NDC: 43742-1272
• Product Type: Human Otc Drug
• Proprietary Name: Cholesterol
• Generic Name: Cholesterinum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2018-10-02
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: CHOLESTEROL
• Active Ingredient Strength: 8 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43742-1272-1

30 mL in 1 BOTTLE, DROPPER (43742-1272-1)

• Marketing Start Date: 2018-10-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-1272-1 [43742127201]

Cholesterol LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-10-02

Drug Details

Active Ingredients

Ingredient	Strength
CHOLESTEROL	8 [hp_X]/mL

OpenFDA Data

• SPL SET ID: f37a57de-b8f8-4b44-9e8c-820979a617d0
• 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