NDC 43742-0218

Apiol

Apiolum

Apiol is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Apiole (parsley).

• Product ID: 43742-0218_3fbaee4a-abc2-4aff-b6e1-e7c91fd03ac6
• NDC: 43742-0218
• Product Type: Human Otc Drug
• Proprietary Name: Apiol
• Generic Name: Apiolum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-04-09
• Marketing End Date: 2021-04-13
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: APIOLE (PARSLEY)
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0218-1

30 mL in 1 BOTTLE, DROPPER (43742-0218-1)

• Marketing Start Date: 2013-04-09
• Marketing End Date: 2021-04-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0218-1 [43742021801]

Apiol LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-04-09
• Marketing End Date: 2021-04-13

Drug Details

Active Ingredients

Ingredient	Strength
APIOLE (PARSLEY)	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 292ed8f7-6b0a-4e27-8bd4-859a2ca1ee49
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • QQ67504PXO

NDC Crossover Matching brand name "Apiol" or generic name "Apiolum"

NDC	Brand Name	Generic Name
43742-0218	Apiol	Apiolum
43742-0781	Apiol	Apiolum
57520-1021	Apiol	Apiolum,
63083-1503	Apiol	Apiol
60512-6184	APIOLUM	APIOLUM