Silicea 6X

Manufacturer
Warsan Homeopathic
Effective date
2020-10-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:34

Label at a glance#

ProductSilicea 6X
Active ingredientSILICON DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Silicea 6X

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 from brittle hair, brittle nails, swelling, seeping wounds, low stamina.

OTC - PURPOSE SECTION

Temporary relief from brittle hair, brittle nails, swelling, seeping wounds, low stamina.

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

silicea 6.jpgsilicea 6.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79718-0057-12022-01-28C16284748780-1d6a99b39-b30c-a426-e053-dadaa90af4c2b2c13d53-67bb-1013-e053-2995a90aa0be

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79718-0057-1Silicea 6X900 in 1 JARTABLET9001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79718-0057SILICEA 6X TABLET [WARSAN HOMEOPATHIC]1Legacy NDC, 1 package rows20201110_b2c13d53-67bb-1013-e053-2995a90aa0be.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
79718-005779718-0057-1
79769-0057

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
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
SILICON DIOXIDEETJ7Z6XBU4ACTIB

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
b2c14151-46c0-0ecc-e053-2995a90a39a4b2c13d53-67bb-1013-e053-2995a90aa0be2020-10-28WarningsExact identifier
spl id: b2c14151-46c0-0ecc-e053-2995a90a39a4
spl set id: b2c13d53-67bb-1013-e053-2995a90aa0be

Reported adverse events (FAERS/openFDA)#

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