NDC 60681-0901

Pleo Selene

Sodium Selenite

Pleo Selene is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Sanum Kehlbeck Gmbh & Co. Kg. The primary component is Sodium Selenite.

• Product ID: 60681-0901_73b79917-67b8-4112-9eec-02adbc2e6e18
• NDC: 60681-0901
• Product Type: Human Otc Drug
• Proprietary Name: Pleo Selene
• Generic Name: Sodium Selenite
• Dosage Form: Solution/ Drops
• Route of Administration: ORAL
• Marketing Start Date: 2010-06-15
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Sanum Kehlbeck GmbH & Co. KG
• Substance Name: SODIUM SELENITE
• Active Ingredient Strength: 4 [hp_X]/30mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 60681-0901-3

1 BOTTLE, DROPPER in 1 CARTON (60681-0901-3) > 30 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2010-06-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60681-0901-3 [60681090103]

Pleo Selene SOLUTION/ DROPS

• Marketing Category: Unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-06-15
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM SELENITE	4 [hp_X]/30mL

OpenFDA Data

• SPL SET ID: 73afb34c-c734-4e00-954d-f49b6941736a
• Manufacturer:
  • Sanum Kehlbeck GmbH & Co. KG
• UNII:
  • HIW548RQ3W