SEPIA OFFICINALIS

Manufacturer
Remedy Makers
Effective date
2010-04-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:02:15

Label at a glance#

ProductSEPIA OFFICINALIS
Active ingredientCUTTLEFISH
Label structure2 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Free from yeast, wheat, corn, and soy.
DIRECTIONS: Dissolve 3 or 4 pellets
in mouth or under tongue 3 times a day or as directed by a physician.
Children 2 years and older take 1/2
adult dose.
INDICATIONS: To be used according
to standard homeopathic indications
for self limiting conditions such as
those indicated on the front panel or as directed by a physician.
Warnings: *Use only if cap and
seal are unbroken. * Keep this and all medications out of reach of children.
* If symptoms persist for more then 3
days, consult your physician.
*As with any drug, if your are pregnant or nursing a baby, seek the advice of a
health professional before using this product.*Store tightly closed in a cool, dark place.
Made according to The Homeopathic Pharmacopoeia of the United States by: Remedy Makers, Pomona, CA 91768

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SEPIA OFFICINALIS 30CSEPIA OFFICINALIS 30C

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10191-1573-22019-10-21C16284748780-1956f9ecf-cc75-621f-e053-dbdaa90a74adSEPIA OFFICINALIS 30C (Cuttlefish)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10191-1573-2SEPIA OFFICINALIS150 in 1 VIAL, GLASSPELLET1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10191-1573SEPIA OFFICINALIS (CUTTLEFISH) PELLET [REMEDY MAKERS]1Legacy NDC, 1 package rows20100409_88001d9b-3194-4c86-85d0-4441fb086ef6.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CUTTLEFISHACTIVE INGREDIENTAFQ8R47WH21
CUTTLEFISHACTIVE MOIETYAFQ8R47WH21

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10191-157310191-1573-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
CUTTLEFISHAFQ8R47WH2ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5be95f06-5af7-4678-8814-ea88925858ec88001d9b-3194-4c86-85d0-4441fb086ef62010-04-08Exact identifier
spl id: 5be95f06-5af7-4678-8814-ea88925858ec
spl set id: 88001d9b-3194-4c86-85d0-4441fb086ef6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.