NDC 10191-1569

SEPIA OFFICINALIS

Cuttlefish

SEPIA OFFICINALIS is a Sublingual Pellet in the Human Otc Drug category. It is labeled and distributed by Remedy Makers. The primary component is Cuttlefish.

• Product ID: 10191-1569_b04dce81-b665-4370-a101-b36fa43850c4
• NDC: 10191-1569
• Product Type: Human Otc Drug
• Proprietary Name: SEPIA OFFICINALIS
• Generic Name: Cuttlefish
• Dosage Form: Pellet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2003-05-07
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Remedy Makers
• Substance Name: CUTTLEFISH
• Active Ingredient Strength: 6 [hp_C]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10191-1569-2

162 PELLET in 1 VIAL, GLASS (10191-1569-2)

• Marketing Start Date: 2003-05-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10191-1569-2 [10191156902]

SEPIA OFFICINALIS PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2003-05-07
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
CUTTLEFISH	6 [hp_C]/1

OpenFDA Data

• SPL SET ID: a489614d-60ca-4eb8-a20b-16fe5294224e
• Manufacturer:
  • Remedy Makers

NDC Crossover Matching brand name "SEPIA OFFICINALIS" or generic name "Cuttlefish"

NDC	Brand Name	Generic Name
10191-1562	SEPIA OFFICINALIS	CUTTLEFISH
10191-1566	SEPIA OFFICINALIS	CUTTLEFISH
10191-1569	SEPIA OFFICINALIS	CUTTLEFISH
10191-1570	SEPIA OFFICINALIS	CUTTLEFISH
10191-1571	SEPIA OFFICINALIS	CUTTLEFISH
10191-1573	SEPIA OFFICINALIS	CUTTLEFISH