NDC 43742-0191

Malvin

Malvin

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

• Product ID: 43742-0191_21c0ee46-0fc5-429b-9cde-c4b0b96a4b1d
• NDC: 43742-0191
• Product Type: Human Otc Drug
• Proprietary Name: Malvin
• Generic Name: Malvin
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2012-10-30
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: MALVIN
• Active Ingredient Strength: 15 [hp_C]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 43742-0191-1

30 mL in 1 BOTTLE, DROPPER (43742-0191-1)

• Marketing Start Date: 2012-10-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0191-1 [43742019101]

Malvin LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-30

Drug Details

Active Ingredients

Ingredient	Strength
MALVIN	15 [hp_C]/mL

OpenFDA Data

• SPL SET ID: e6788c9c-8596-4179-92ba-23774a95165c
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • I9I120531L

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

NDC	Brand Name	Generic Name
43742-0191	Malvin	Malvin
63083-1525	Malvin	Malvin