FDA.reportPublic FDA data

Populus 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 17:50:51

Label at a glance#

ProductPopulus Combination 9236
Active ingredientPOPULUS TREMULOIDES BARK, SAW PALMETTO, APIS MELLIFERA, BAPTISIA TINCTORIA WHOLE, CAMPHOR (NATURAL), CAPSICUM, PIPER CUBEBA FRUIT, EQUISETUM HYEMALE WHOLE, ONONIS REPENS WHOLE, RUBIA TINCTORUM ROOT, SCROPHULARIA NODOSA WHOLE, SOLIDAGO VIRGAUREA FLOWERING TOP, URTICA URENS WHOLE, ARCTOSTAPHYLOS TOMENTOSA WHOLE, PETROSELINUM CRISPUM ROOT, BERBERIS VULGARIS ROOT BARK, LYTTA VESICATORIA, AGATHOSMA BETULINA LEAF, WOOD CREOSOTE, DRIMIA MARITIMA BULB, TURPENTINE OIL, MERCURIC CHLORIDE
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

Populus tremuloides 1X
Sabal serrulata 1X
Apis mellifica 3X
Baptisia tinctoria 3X
Camphora 3X
Capsicum annuum 3X
Cubeba officinalis 3X
Equisetum hyemale 3X
Ononis spinosa 3X
Rubia tinctorum 3X
Scrophularia nodosa 3X
Solidago virgaurea 3X
Urtica urens 3X
Uva-ursi 3X
Petroselinum sativum 4X
Berberis vulgaris 5X
Cantharis 5X
Barosma crenata 6X
Kreosotum 6X
Scilla maritima 6X
Terebinthina 6X
Mercurius corrosivus 12X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of constipation, diarrhea, or frequent urination.*

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

Populus Combination

Homeopathic Remedy

1 FL. OZ. (29.5 mL)

Label imageLabel image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-9236-12026-01-09C16284748780-11030e365-3612-111a-e063-dadaa90a10e2R236
63083-9236-12026-01-09C16284748780-11030e365-3612-111a-e063-dadaa90a10e2R236
63083-9236-12024-01-30C16284748780-11030e365-3612-111a-e063-dadaa90a10e2R236
63083-9236-12024-01-30C16284748780-11030e365-3612-111a-e063-dadaa90a10e2R236

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-9236-1Populus Combination923629.5 mL in 1 BOTTLE, DROPPERLIQUID29.52

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-923663083-9236-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
POPULUS TREMULOIDES BARK5543O0CEIDACTIB
SAW PALMETTOJ7WWH9M8QSACTIB
APIS MELLIFERA7S82P3R43ZACTIB
BAPTISIA TINCTORIA WHOLE5K1UO2888YACTIB
CAMPHOR (NATURAL)N20HL7Q941ACTIB
CAPSICUM00UK7646FGACTIB
PIPER CUBEBA FRUITZ99L7429MAACTIB
EQUISETUM HYEMALE WHOLE59677RXH25ACTIB
ONONIS REPENS WHOLE7J37EHM6J6ACTIB
RUBIA TINCTORUM ROOT0SVP95L23GACTIB
SCROPHULARIA NODOSA WHOLE7H443NUB2TACTIB
SOLIDAGO VIRGAUREA FLOWERING TOP5405K23S50ACTIB
URTICA URENS WHOLEIHN2NQ5OF9ACTIB
ARCTOSTAPHYLOS TOMENTOSA WHOLE0N0F73S1JOACTIB
PETROSELINUM CRISPUM ROOT030FN29S9HACTIB
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
LYTTA VESICATORIA3Q034RO3BTACTIB
AGATHOSMA BETULINA LEAF369DDH39Z0ACTIB
WOOD CREOSOTE3JYG22FD73ACTIB
DRIMIA MARITIMA BULB3629601H5DACTIB
TURPENTINE OILC5H0QJ6V7FACTIB
MERCURIC CHLORIDE53GH7MZT1RACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:15:53

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
Populus Combination 9236POPULUS COMBINATIONProfessional Complementary Health Formulasb24596b6-8e15-40d4-8800-39c8160e61f32026-01-08WarningsExact identifier
ndc (package): 63083-9236-1
ndc (product): 63083-9236
ndc11 (package): 63083923601
spl id: b691542e-a8c1-4e32-b460-7a0e2dfbade8
spl set id: b24596b6-8e15-40d4-8800-39c8160e61f3

Reported adverse events (FAERS/openFDA)#

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