FDA.reportPublic FDA data

WHP Hot Flashes

Manufacturer
Washington Homeopathic Products
Effective date
2025-01-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:31:36

Label at a glance#

ProductWHP Hot Flashes
Active ingredientSULFUR, LACHESIS MUTA VENOM, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE
Label structure8 sections

Indications and uses

Temporarily relieves hot flashes and other symptoms associated with change of life.

Dosage and administration

Directions: Adults and children 12 years and older: 2 pills dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children 4 years to under 12 years: 1 pill dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children under 4 years: Consult a licensed practitioner.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

LACHESIS 6C

PULSATILLA 6C

SEPIA 12C

SULPHUR 6C

USES

OTC - PURPOSE SECTION

Temporarily relieves hot flashes and other symptoms associated with change of life.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

As with all medications, keep out of reach of children.

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist or recur, discontinue use. If pregnant or nursing, consult a licensed practitioner before using this product.

INDICATIONS

INDICATIONS & USAGE SECTION

LACHESIS Sore throat

PULSATILLA Weeping

SEPIA Indifference

SULPHUR Agitation

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Directions: Adults and children 12 years and older: 2 pills dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children 4 years to under 12 years: 1 pill dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children under 4 years: Consult a licensed practitioner.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WHP Hot Flashes labelWHP Hot Flashes labelWHP Hot Flashes boxWHP Hot Flashes box

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71919-808-14WHP Hot Flashes1 in 1 BOXPELLET12
71919-808-14WHP Hot Flashes1 in 1 BOTTLE, PLASTICPELLET12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71919-808WHP HOT FLASHES (LACHESIS MUTA VENOM - PULSATILLA VULGARIS - SEPIA OFFICINALIS JUICE - SULFUR) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]2Current NDC, 2 package rows20250130_06d5e51f-78ab-72c7-e063-6394a90a9ab1.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71919-80871919-808-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
LACTOSEJ2B2A4N98GIACT
SULFUR70FD1KFU70ACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB

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
WHP Hot FlashesLACHESIS MUTA VENOM - PULSATILLA VULGARIS - SEPIA OFFICINALIS JUICE - SULFURWashington Homeopathic Products06d5e51f-78ab-72c7-e063-6394a90a9ab12025-01-28WarningsExact identifier
ndc (package): 71919-808-14
ndc (product): 71919-808
ndc11 (package): 71919080814
spl id: 2cc864a3-46c8-252b-e063-6294a90aad58
spl set id: 06d5e51f-78ab-72c7-e063-6394a90a9ab1

Reported adverse events (FAERS/openFDA)#

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