Sepia Combination

Manufacturer
Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing LLC
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:50:23

Label at a glance#

ProductSepia Combination 9246
Active ingredientPOTASSIUM BROMIDE, STRYCHNOS IGNATII SEED, PHOSPHORIC ACID, SEPIA OFFICINALIS JUICE, ZINC VALERATE DIHYDRATE, SCABIES LESION LYSATE (HUMAN)
Label structure9 sections

Dosage and administration

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Kali bromatum 4X
Ignatia amara 4X
Phosphoricum acidum 4X
Sepia 4X
Zincum valerianicum 8X
Psorinum 12X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of mental fatigue or exhaustion, anxiousness, or insomnia.*

OTC - PURPOSE SECTION

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS

WARNINGS SECTION

Consult a doctor if condition worsens or if symptoms persist. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

OTHER SAFETY INFORMATION

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

40% ethanol, purified water.

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est 1985

Professional Formulas

Complementary Health

Sepia Combination

Homeopathic Remedy

1 FL. OZ. (29.5 mL)

Label imageLabel image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-9246-12026-01-08C16284748780-11030e365-3be7-111a-e063-dadaa90a10e2R246
63083-9246-12026-01-08C16284748780-11030e365-3be7-111a-e063-dadaa90a10e2R246
63083-9246-12024-01-30C16284748780-11030e365-3be7-111a-e063-dadaa90a10e2R246
63083-9246-12024-01-30C16284748780-11030e365-3be7-111a-e063-dadaa90a10e2R246

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-9246-1Sepia Combination924629.5 mL in 1 BOTTLE, DROPPERLIQUID29.52

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-924663083-9246-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:15:54

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
Sepia Combination 9246SEPIA COMBINATIONProfessional Complementary Health Formulasfe79986b-7b2d-4cfd-8386-45de02115ca92026-01-08WarningsExact identifier
ndc (package): 63083-9246-1
ndc (product): 63083-9246
ndc11 (package): 63083924601
spl id: 06b7e030-310d-4195-90ad-6d7ed17e2adb
spl set id: fe79986b-7b2d-4cfd-8386-45de02115ca9

Reported adverse events (FAERS/openFDA)#

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