Pulsatilla 30X

Manufacturer
True Botanica, LLC
Effective date
2025-03-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:32:14

Label at a glance#

ProductPulsatilla 30X
Active ingredientPULSATILLA VULGARIS
Label structure11 sections

Dosage and administration

Place drops under tongue for 30 seconds. Adults 7 drops 3 times a day. Children 2-12 years, 7 drops 3 times a day. Under 2 years, consult your doctor. Use until symptoms are relieved or as directed by your health care provider.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Pulsatilla vulgaris 30X

OTC - PURPOSE SECTION

For temporary relief of a timid, weepy disposition, ear discharge, loss of smell. May also be used for standard homeopathic indications or as directed by your physician.

Use:

INDICATIONS & USAGE SECTION

For temporary relief of a timid, weepy disposition, ear discharge, loss of smell. May also be used for standard homeopathic indications or as directed by your physician.

Warnings:

WARNINGS SECTION

Consult your health care provider if symptoms persist more than 5 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTC - DO NOT USE SECTION

TAMPER EVIDENT: Do not use if safety seal is broken before first use.

Directions for Use:

DOSAGE & ADMINISTRATION SECTION

Place drops under tongue for 30 seconds. Adults 7 drops 3 times a day. Children 2-12 years, 7 drops 3 times a day. Under 2 years, consult your doctor. Use until symptoms are relieved or as directed by your health care provider.

Other Ingredients:

INACTIVE INGREDIENT SECTION

Citric Acid, Potassium Sorbate, Water

OTC - QUESTIONS SECTION

Developed and Made by

True Botanica, LLC

1005 Richards Rd., Suite D

Hartland, WI 53029

800-315-8783

www.truebotanica.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pulsatilla 30X_30ml_V1Pulsatilla 30X_30ml_V1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53645-1982-6Pulsatilla 30X30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53645-1982PULSATILLA 30X (PULSATILLA VULGARIS) LIQUID [TRUE BOTANICA, LLC]1Current NDC, 1 package rows20250306_2bae8d35-1724-f1f4-e063-6294a90a374c.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53645-198253645-1982-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
Pulsatilla 30XPULSATILLA VULGARISTrue Botanica, LLC2bae8d35-1724-f1f4-e063-6294a90a374c2025-03-03WarningsExact identifier
ndc (package): 53645-1982-6
ndc (product): 53645-1982
ndc11 (package): 53645198206
spl id: 2bae9207-48c9-cd77-e063-6394a90aa4b8
spl set id: 2bae8d35-1724-f1f4-e063-6294a90a374c

Reported adverse events (FAERS/openFDA)#

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