Kali Phos 12X

Manufacturer
Warsan Homeopathic
Effective date
2020-10-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:32

Label at a glance#

ProductKali Phos 12X
Active ingredientPOTASSIUM PHOSPHATE, UNSPECIFIED FORM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Kali Phos 12X

INACTIVE INGREDIENT SECTION

Lactose

WARNINGS SECTION

Stop use and ask doctor if symptoms worsen or persist longer than 7 days.

Do not use if tamper evident seal is missing or broken.

INDICATIONS & USAGE SECTION

Temporary relief fatigue, weakness, exhaustion.

OTC - PURPOSE SECTION

Temporary relief fatigue, weakness, exhaustion.

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: Four tablets every thirty minutes for six doses followed by four tablets every 4-6 hours as needed.

Children 2 years to 12 years of age: Four tablets every thirty minutes for six doses followed by two tablets every 4-6 hours as needed.

Children under 2 years of age: Consult doctor prior to use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

kali phos 12.jpgkali phos 12.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79718-0028-12022-01-28C16284748780-1d6a99b39-b324-a426-e053-dadaa90af4c2b2b1312b-da0b-b9d4-e053-2995a90a421a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79718-0028-1Kali Phos 12X100 in 1 JARTABLET1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79718-0028KALI PHOS 12X TABLET [WARSAN HOMEOPATHIC]1Legacy NDC, 1 package rows20201110_b2b1312b-da0b-b9d4-e053-2995a90a421a.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
79718-002879718-0028-1
79769-0028

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 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
b2b13134-d16e-b7dd-e053-2995a90a8112b2b1312b-da0b-b9d4-e053-2995a90a421a2020-10-27WarningsExact identifier
spl id: b2b13134-d16e-b7dd-e053-2995a90a8112
spl set id: b2b1312b-da0b-b9d4-e053-2995a90a421a

Reported adverse events (FAERS/openFDA)#

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