FDA.reportPublic FDA data

Southwest Regional

Manufacturer
Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing
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#

ProductSouthwest Regional 1020
Active ingredientSUS SCROFA ADRENAL GLAND, CORTICOTROPIN, HISTAMINE DIHYDROCHLORIDE, BEEF LIVER, POPULUS FREMONTII POLLEN, FRAXINUS LATIFOLIA WHOLE, POPULUS TREMULOIDES POLLEN, SUAEDA MARITIMA FLOWERING TOP, CYNODON DACTYLON WHOLE, BETULA OCCIDENTALIS POLLEN, ACER NEGUNDO ROOT BARK, BASSIA SCOPARIA FRUIT, XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN, BACCHARIS PILULARIS WHOLE, ELM, MEDICAGO SATIVA WHOLE, CARYA LACINIOSA BARK, JUNIPERUS SCOPULORUM POLLEN, CHENOPODIUM ALBUM POLLEN, IVA ANGUSTIFOLIA WHOLE, PROSOPIS CINERARIA WOOD, EPHEDRA NEVADENSIS WHOLE, WHITE MULBERRY, QUERCUS KELLOGGII POLLEN, OLEA EUROPAEA FLOWER, CITRUS SINENSIS POLLEN, PECAN, AMARANTHUS HYBRIDUS LEAF, PINUS PONDEROSA POLLEN, PINUS CEMBROIDES POLLEN, PLANTAGO AUSTRALIS WHOLE, LIGUSTRUM LUCIDUM SEED, AMBROSIA ARTEMISIIFOLIA WHOLE, RUMEX CRISPUS ROOT, SALSOLA KALI WHOLE, SAGE, TAMARIX GALLICA POLLEN, SYMPHORICARPOS ALBUS FRUIT, ENGLISH WALNUT, AMARANTHUS TUBERCULATUS POLLEN, SALIX LUTEA POLLEN
Label structure9 sections

Dosage and administration

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 to 15 drops up to 3 times per day. For desensitization, begin with 1 to 5 drops daily, increasing to the standard dose gradually to avoid symptom expression; after 1 to 3 months at the standard dose, decrease gradually to a maintenance dose of 10 to 15 drops weekly. Consult a physician for use in children under 1...

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Adrenal 6X
ACTH 6X, 30X
Histaminum hydrochloricum 12X
Liver 6X, 12X
and all the following at 6X, 12X, 60X, 100X:
Arizona cottonwood
Ash
Aspen
Atriplex
Bermuda grass
Birch/alder mix
Box elder
Burning bush
Cocklebur
Coyote brush
Elm
Grass mix
Hickory
Juniper
Lamb's quarters
Marsh elder
Mesquite
Mormon tea
Mountain cedar
Mulberry
Oak
Olive pollen
Orange pollen
Pecan
Pigweed mix
Pine
Pinion
Plantain
Privet
Ragweed
Rocky Mountain juniper
Rumex mix
Russian thistle
Sage
Salt cedar
Sycamore
Walnut
Waterhemp
Willow

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of runny nose, sneezing, itching of the nose or throat, and itchy, watery eyes due to sensitivity to common allergens of the southwestern United States.*

OTC - PURPOSE SECTION

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

WARNINGS

WARNINGS SECTION

In case of overdose, get medical help or contact a poison control center right away.

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 to 15 drops up to 3 times per day. For desensitization, begin with 1 to 5 drops daily, increasing to the standard dose gradually to avoid symptom expression; after 1 to 3 months at the standard dose, decrease gradually to a maintenance dose of 10 to 15 drops weekly. 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

20% ethanol, purified water.

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est 1985

Professional Formulas

Complementary Health

Southwest Regional

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label imageLabel image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7314d8f7-fa99-4dc2-9f68-de2ff142f4b7Product name220250121

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-1020-22026-01-09C16284748780-11030e365-1572-111a-e063-dadaa90a10e2ASW
63083-1020-22026-01-09C16284748780-11030e365-1572-111a-e063-dadaa90a10e2ASW
63083-1020-22024-01-30C16284748780-11030e365-1572-111a-e063-dadaa90a10e2ASW
63083-1020-22024-01-30C16284748780-11030e365-1572-111a-e063-dadaa90a10e2ASW

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-1020-2Southwest Regional102059 mL in 1 BOTTLE, DROPPERLIQUID592

Products#

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

DailyMed product names page 1 of 2 · 46 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-102063083-1020-2

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 43 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
CORTICOTROPINK0U68Q2TXAACTIB
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
BEEF LIVERW8N8R55022ACTIB
POPULUS FREMONTII POLLEN426RHB4302ACTIB
FRAXINUS LATIFOLIA WHOLE024W88F557ACTIB
POPULUS TREMULOIDES POLLEN928OC2TJDAACTIB
SUAEDA MARITIMA FLOWERING TOP0K803ZTV5NACTIB
CYNODON DACTYLON WHOLE2Q8MR21NHKACTIB
BETULA OCCIDENTALIS POLLENR889N2L976ACTIB
ACER NEGUNDO ROOT BARK56W138ID6KACTIB
BASSIA SCOPARIA FRUIT04W97Z676YACTIB
XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN0ZK6G3W3BIACTIB
BACCHARIS PILULARIS WHOLEU8I5N8Q01BACTIB
ELM63POE2M46YACTIB
MEDICAGO SATIVA WHOLEDJO934BRBDACTIB
CARYA LACINIOSA BARK98Q86P6WFRACTIB
JUNIPERUS SCOPULORUM POLLEN0G82TT8ZFYACTIB
CHENOPODIUM ALBUM POLLEN098LKX5NCNACTIB
IVA ANGUSTIFOLIA WHOLE1BTG48T6EAACTIB
PROSOPIS CINERARIA WOOD06ZPE0373LACTIB
EPHEDRA NEVADENSIS WHOLE046PB542M7ACTIB
WHITE MULBERRYMN25R0HH5AACTIB
QUERCUS KELLOGGII POLLEN02RVY6X9ECACTIB
OLEA EUROPAEA FLOWER498M34P1VZACTIB
CITRUS SINENSIS POLLEN0U790UB32KACTIB
PECANF14P91GB5FACTIB
AMARANTHUS HYBRIDUS LEAF07L86FJ69JACTIB
PINUS PONDEROSA POLLEN042SUA2DS9ACTIB
PINUS CEMBROIDES POLLEN956F61CB2VACTIB
PLANTAGO AUSTRALIS WHOLE0008D0X3XIACTIB
LIGUSTRUM LUCIDUM SEED1A3CS89UKDACTIB
AMBROSIA ARTEMISIIFOLIA WHOLE9W34L2CQ9AACTIB
RUMEX CRISPUS ROOT9N1RM2S62CACTIB
SALSOLA KALI WHOLE0BKP293XE9ACTIB
SAGE065C5D077JACTIB
TAMARIX GALLICA POLLEN43IR7KR479ACTIB
SYMPHORICARPOS ALBUS FRUIT873JZU3ASZACTIB
ENGLISH WALNUT1V3SHR7QB7ACTIB
AMARANTHUS TUBERCULATUS POLLEN92N6W6KO2GACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:15:41

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
Southwest Regional 1020SOUTHWEST REGIONALProfessional Complementary Health Formulasaef52f46-bae8-4e1c-9ac2-067ab8d7369f2026-01-08WarningsExact identifier
ndc (package): 63083-1020-2
ndc (product): 63083-1020
ndc11 (package): 63083102002
spl id: af0838bc-a446-4872-a4ba-cc64363a2b6a
spl set id: aef52f46-bae8-4e1c-9ac2-067ab8d7369f

Reported adverse events (FAERS/openFDA)#

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