Kalium Sulfuratum Bath Essence

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-01-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:25:59

Label at a glance#

ProductKalium Sulfuratum Bath Essence
Active ingredientSULFUR
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

For compresses: Use 2 teaspoons per cup of lukewarm water. For full bath: Use 2-3 tablespoons.

SHAKE WELL BEFORE USE.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Kalium sulfuratum (Potassium polysulfide) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Spring water

"prepared using rhythmical processes"

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: FOR EXTERNAL USE ONLY.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kalium sulfuratum Bath Essence LiquidKalium sulfuratum Bath Essence Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-6071-6Kalium Sulfuratum Bath Essence125 mL in 1 BOTTLE, GLASSLIQUID1252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-6071KALIUM SULFURATUM BATH ESSENCE LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20240207_6ba0600c-03c2-e39b-e053-2a91aa0a6234.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-607148951-6071-6

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SULFUR70FD1KFU70ACTIB
WATER059QF0KO0RIACT

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
104474da-39e7-dcc3-e063-6394a90a11516ba0600c-03c2-e39b-e053-2a91aa0a62342024-01-31WarningsExact identifier
spl id: 104474da-39e7-dcc3-e063-6394a90a1151
spl set id: 6ba0600c-03c2-e39b-e053-2a91aa0a6234

Reported adverse events (FAERS/openFDA)#

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