NDC 43742-0212

Indole

Indolum

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

• Product ID: 43742-0212_81a42657-5fbd-4ba1-b29b-8035c1dda385
• NDC: 43742-0212
• Product Type: Human Otc Drug
• Proprietary Name: Indole
• Generic Name: Indolum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-04-03
• Marketing End Date: 2020-08-24
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: INDOLE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0212-1

30 mL in 1 BOTTLE, DROPPER (43742-0212-1)

• Marketing Start Date: 2013-04-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0212-1 [43742021201]

Indole LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-04-03
• Marketing End Date: 2020-08-24

Drug Details

Active Ingredients

Ingredient	Strength
INDOLE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 23e6083c-2325-43f4-b833-9ff8e33f0030
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 8724FJW4M5

NDC Crossover Matching brand name "Indole" or generic name "Indolum"

NDC	Brand Name	Generic Name
43742-0212	Indole	Indolum
43742-0818	Indole	Indolum
44911-0435	Indole Phenolic	Indolum