NDC 43742-0185

Coniferyl Alcohol

Coniferyl Alcohol

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

• Product ID: 43742-0185_0a5b5d9e-9692-4a7c-b9eb-cdf6cad02613
• NDC: 43742-0185
• Product Type: Human Otc Drug
• Proprietary Name: Coniferyl Alcohol
• Generic Name: Coniferyl Alcohol
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2012-10-29
• Marketing End Date: 2021-11-22
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: CONIFERYL ALCOHOL
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0185-1

30 mL in 1 BOTTLE, DROPPER (43742-0185-1)

• Marketing Start Date: 2012-10-29
• Marketing End Date: 2021-11-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0185-1 [43742018501]

Coniferyl Alcohol LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-29
• Marketing End Date: 2021-11-22

Drug Details

Active Ingredients

Ingredient	Strength
CONIFERYL ALCOHOL	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: b29374ac-eaa8-43ac-afbf-6bc114583fc2
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • E7SM92591P

NDC Crossover Matching brand name "Coniferyl Alcohol" or generic name "Coniferyl Alcohol"

NDC	Brand Name	Generic Name
43742-0185	Coniferyl Alcohol	Coniferyl Alcohol
43857-0368	Coniferyl Alcohol	Coniferyl Alcohol
63083-1512	Coniferyl Alcohol	Coniferyl Alcohol
44911-0253	Coniferyl Alcohol Phenolic	Coniferyl Alcohol