NDC 10191-1571

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 Sepia Officinalis Juice.

• Product ID: 10191-1571_47facc8a-4782-402d-ae23-4fa442287240
• NDC: 10191-1571
• Product Type: Human Otc Drug
• Proprietary Name: SEPIA OFFICINALIS
• Generic Name: Cuttlefish
• Dosage Form: Pellet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2003-04-23
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: REMEDY MAKERS
• Substance Name: SEPIA OFFICINALIS JUICE
• Active Ingredient Strength: 12 [hp_C]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10191-1571-2

136 PELLET in 1 VIAL, GLASS (10191-1571-2)

• Marketing Start Date: 2003-04-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10191-1571-2 [10191157102]

SEPIA OFFICINALIS PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2003-04-23
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
SEPIA OFFICINALIS JUICE	12 [hp_C]/1

OpenFDA Data

• SPL SET ID: db88b67f-d269-4886-8d53-19afe527239f
• Manufacturer:
  • REMEDY MAKERS
• UNII:
  • QDL83WN8C2
• UPC Code:
  • 0310191157125

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