FDA.reportPublic FDA data

Selenium 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 17:50:40

Label at a glance#

ProductSelenium Combination 9245
Active ingredientRHODODENDRON TOMENTOSUM LEAFY TWIG, URTICA URENS WHOLE, HORSE CHESTNUT, ARCTIUM LAPPA ROOT OIL, CALCIUM FLUORIDE, GALIUM APARINE WHOLE, STRYCHNOS IGNATII SEED, PHOSPHORIC ACID, SULFUR, THUJA OCCIDENTALIS LEAF, OXOGLURIC ACID, FUMARIC ACID, BEEF KIDNEY, BEEF LIVER, SODIUM DIETHYL OXALACETATE, BOS TAURUS PLACENTA, SELENIUM, CHICKEN SKIN, COOKED, BOS TAURUS SPLEEN, AMMONIUM Cation, MERCURIUS SOLUBILIS, CORTISONE ACETATE, FORMIC ACID
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

Ledum palustre 4X
Urtica urens 4X
Aesculus hippocastanum 6X
Arctium lappa 6X
Calcarea fluorica 6X
Galium aparine 6X
Ignatia amara 6X
Phosphoricum acidum 6X
Sulphur 8X
Thuja occidentalis 8X
a-Ketoglutaricum acidum 10X
Fumaricum acidum 10X
Kidney 10X
Liver 10X
Natrum oxalaceticum 10X
Placenta 10X
Selenium metallicum 10X
Skin 10X
Spleen 10X
Sanguinarinum nitricum 12X
Mercurius solubilis 13X
Cortisone aceticum 28X
Formicum acidum 198X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of mild skin inflammation such as eczema, acne, or dermatitis.*

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

Selenium Combination

Homeopathic Remedy

1 FL. OZ. (29.5 mL)

Label imageLabel image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
86fffa7b-d382-4771-a253-25cccb64b590Product name320251124
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
9bfd9c37-f773-6e9a-5f6b-6f5701d62adcProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-9245-12026-01-09C16284748780-11030e365-5786-111a-e063-dadaa90a10e2R245
63083-9245-12026-01-09C16284748780-11030e365-5786-111a-e063-dadaa90a10e2R245
63083-9245-12024-01-30C16284748780-11030e365-5786-111a-e063-dadaa90a10e2R245
63083-9245-12024-01-30C16284748780-11030e365-5786-111a-e063-dadaa90a10e2R245

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-9245-1Selenium Combination924529.5 mL in 1 BOTTLE, DROPPERLIQUID29.52

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-924563083-9245-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
RHODODENDRON TOMENTOSUM LEAFY TWIG877L01IZ0PACTIB
URTICA URENS WHOLEIHN2NQ5OF9ACTIB
HORSE CHESTNUT3C18L6RJAZACTIB
ARCTIUM LAPPA ROOT OIL55DGS3F5YGACTIB
CALCIUM FLUORIDEO3B55K4YKIACTIB
GALIUM APARINE WHOLEZ4B6561488ACTIB
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
SULFUR70FD1KFU70ACTIB
THUJA OCCIDENTALIS LEAF0T0DQN8786ACTIB
OXOGLURIC ACID8ID597Z82XACTIB
FUMARIC ACID88XHZ13131ACTIB
BEEF KIDNEY5HOC10FSICACTIB
BEEF LIVERW8N8R55022ACTIB
SODIUM DIETHYL OXALACETATE6CA025Y4FGACTIB
BOS TAURUS PLACENTA83AL37E3A7ACTIB
SELENIUMH6241UJ22BACTIB
CHICKEN SKIN, COOKED00GG7UT6PLACTIB
BOS TAURUS SPLEEN190Q9MB3U3ACTIB
AMMONIUM Cation54S68520I4ACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
CORTISONE ACETATE883WKN7W8XACTIB
FORMIC ACID0YIW783RG1ACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:15:47

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
Selenium Combination 9245SELENIUM COMBINATIONProfessional Complementary Health Formulas1c2cc0ad-f859-470b-be4b-f98e010a2e5c2026-01-08WarningsExact identifier
ndc (package): 63083-9245-1
ndc (product): 63083-9245
ndc11 (package): 63083924501
spl id: e2ac054e-dc6c-4e19-bde5-7a038998d0c9
spl set id: 1c2cc0ad-f859-470b-be4b-f98e010a2e5c

Reported adverse events (FAERS/openFDA)#

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