FDA.reportPublic FDA data

Gun Powder

Manufacturer
Warsan Homeopathic
Effective date
2020-12-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:04

Label at a glance#

ProductGun Powder
Active ingredientPOTASSIUM NITRATE, ACTIVATED CHARCOAL, SULFUR
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Potassium Nitrate 3X, Charcoal 3X, Sulphur 3X

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 skin problems, boils, cuts, deep injuries, animal bites

OTC - PURPOSE SECTION

Temporary relief of skin problems, boils, cuts, deep injuries, animal bites

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: Take 2 talbets three times a day or as prescribed by doctor.

Children 2 years to 12 years of age: Take 1-2 tablets two to three time pers day or as prescribed by doctor.

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

gunpowder.jpggunpowder.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79718-0061-12022-01-28C16284748780-1d6a99b39-b593-a426-e053-dadaa90af4c2b636e726-0b11-8eb7-e053-2995a90a1fcb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79718-0061-1Gun Powder900 in 1 JARTABLET9001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79718-0061GUN POWDER TABLET [WARSAN HOMEOPATHIC]1Legacy NDC, 1 package rows20201231_b636e726-0b11-8eb7-e053-2995a90a1fcb.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79718-006179718-0061-1
79769-0061

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
POTASSIUM NITRATERU45X2JN0ZACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
SULFUR70FD1KFU70ACTIB

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
b636e726-0b12-8eb7-e053-2995a90a1fcbb636e726-0b11-8eb7-e053-2995a90a1fcb2020-12-11WarningsExact identifier
spl id: b636e726-0b12-8eb7-e053-2995a90a1fcb
spl set id: b636e726-0b11-8eb7-e053-2995a90a1fcb

Reported adverse events (FAERS/openFDA)#

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