NDC 57520-1021

Apiol

Apiolum,

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

• Product ID: 57520-1021_0cafdd55-113c-4e74-a2d9-025a12bbf555
• NDC: 57520-1021
• Product Type: Human Otc Drug
• Proprietary Name: Apiol
• Generic Name: Apiolum,
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2011-12-13
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Apotheca Company
• Substance Name: APIOLE (PARSLEY)
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 57520-1021-1

30 mL in 1 BOTTLE, DROPPER (57520-1021-1)

• Marketing Start Date: 2011-12-13
• Marketing End Date: 2022-12-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 57520-1021-1 [57520102101]

Apiol LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-13
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

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

OpenFDA Data

• SPL SET ID: 0d23e0d9-4254-4623-b27a-e811041ff930
• Manufacturer:
  • Apotheca Company
• 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