NDC 60681-7002

Pleo Cerivi

Cetraria Islandica Subsp. Islandica

Pleo Cerivi is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Sanum Kehlbeck Gmbh & Co. Kg. The primary component is Cetraria Islandica Subsp. Islandica.

• Product ID: 60681-7002_2d067039-1b84-4400-8021-baacc4a92a7a
• NDC: 60681-7002
• Product Type: Human Otc Drug
• Proprietary Name: Pleo Cerivi
• Generic Name: Cetraria Islandica Subsp. Islandica
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 1998-01-19
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Sanum Kehlbeck GmbH & Co. KG
• Substance Name: CETRARIA ISLANDICA SUBSP. ISLANDICA
• Active Ingredient Strength: 3 [hp_X]/2mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 60681-7002-2

50 VIAL, GLASS in 1 CARTON (60681-7002-2) > 1 mL in 1 VIAL, GLASS

• Marketing Start Date: 1998-01-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60681-7002-2 [60681700202]

Pleo Cerivi LIQUID

• Marketing Category: UNAPPROVED HOMEOPATHIC
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1998-01-19
• Inactivation Date: 2019-10-21

NDC 60681-7002-1 [60681700201]

Pleo Cerivi LIQUID

• Marketing Category: UNAPPROVED HOMEOPATHIC
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1998-01-19
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
CETRARIA ISLANDICA SUBSP. ISLANDICA	3 [hp_X]/2mL

OpenFDA Data

• SPL SET ID: b22792ef-0ebe-4857-a363-c2064910a0ea
• Manufacturer:
  • Sanum Kehlbeck GmbH & Co. KG
• UNII:
  • BJ7YPN79A1

NDC Crossover Matching brand name "Pleo Cerivi" or generic name "Cetraria Islandica Subsp. Islandica"

NDC	Brand Name	Generic Name
60681-7001	Pleo Cerivi	Cetraria islandica subsp. islandica
60681-7002	Pleo Cerivi	Cetraria islandica subsp. islandica