FDA.reportPublic FDA data

Baptisia Tinctoria Kit Refill

Manufacturer
Washington Homeopathic Products
Effective date
2025-01-28
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:31:41

Label at a glance#

ProductBaptisia Tinctoria Kit Refill
Active ingredientBAPTISIA TINCTORIA ROOT
Label structure7 sections

Indications and uses

To relieve the symptoms of flu-like symptoms.

Dosage and administration

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

Label contents#

Full prescribing information#

USES

OTC - PURPOSE SECTION

To relieve the symptoms of flu-like symptoms.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

Indications:

BAPTISIA TINCTORIA Flu-like symptoms

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71919-765-01Baptisia Tinctoria Kit Refill350 in 1 VIAL, GLASSPELLET3504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71919-765BAPTISIA TINCTORIA KIT REFILL (BAPTISIA TINCTORIA ROOT) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]4Current NDC, Legacy NDC, 1 package rows20250130_dead18ed-a4ba-8129-e053-2a95a90a3f2e.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71919-76571919-765-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
LACTOSEJ2B2A4N98GIACT
BAPTISIA TINCTORIA ROOT5EF0HWI5WUACTIB

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
Baptisia Tinctoria Kit RefillBAPTISIA TINCTORIA ROOTWashington Homeopathic Productsdead18ed-a4ba-8129-e053-2a95a90a3f2e2025-01-28WarningsExact identifier
ndc (package): 71919-765-01
ndc (product): 71919-765
ndc11 (package): 71919076501
spl id: 2cc7eaaf-e2c6-f06a-e063-6394a90a1961
spl set id: dead18ed-a4ba-8129-e053-2a95a90a3f2e

Reported adverse events (FAERS/openFDA)#

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