NDC 10191-1566

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: 10191-1566_3c2e96aa-70fb-4a33-8509-34c03ac22548
• NDC: 10191-1566
• Product Type: Human Otc Drug
• Proprietary Name: SEPIA OFFICINALIS
• Generic Name: Cuttlefish
• Dosage Form: Pellet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2000-02-21
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: REMEDY MAKERS
• Substance Name: SEPIA OFFICINALIS JUICE
• Active Ingredient Strength: 30 [hp_X]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10191-1566-2

164 PELLET in 1 VIAL, GLASS (10191-1566-2)

• Marketing Start Date: 2000-02-21
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10191-1566-2 [10191156602]

SEPIA OFFICINALIS PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2000-02-21
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
SEPIA OFFICINALIS JUICE	30 [hp_X]/1

OpenFDA Data

• SPL SET ID: 4bed4705-a8bf-423d-99ca-02bb5e2cbeab
• Manufacturer:
  • REMEDY MAKERS
• UNII:
  • QDL83WN8C2
• UPC Code:
  • 0310191156623

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