FDA.reportPublic FDA data

Natrum sulphuricum 30C

Manufacturer
Paramesh Banerji Life Sciences LLC
Effective date
2015-06-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:07:58

Label at a glance#

ProductNatrum sulphuricum 30C
Active ingredientSODIUM SULFATE
Label structure9 sections

Indications and uses

Helps improve suppurative ulcers

Label contents#

Full prescribing information#

DRUG FACTS: Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Natrum sulphuricum 30C HPUS

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sucrose, Lactose

Purpose

OTC - PURPOSE SECTION

Helps improve suppurative ulcers

Uses

INDICATIONS & USAGE SECTION

Helps improve suppurative ulcers

Warnings

WARNINGS SECTION

If pregnant or breast feeding ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Direction

DOSAGE & ADMINISTRATION SECTION

Adult or child: Take three pills daily. Leaving a gap of 30 minutes after any food or as advised by your physician.

Manufactured by

SPL UNCLASSIFIED SECTION

Paramesh Banerji Life Sciences, LLC.

North Brunswick, NJ 08902, USA.

Tel: +1-732-743-5936,

Email: info@pblifesciences.com

www.pblifesciences.com/permapotent

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Natrum sulphuricum 30CNatrum sulphuricum 30C

NDC: 69152-1167-1

Natrum sulphuricum 30C

Homeopathic Medicine

Helps improve suppurative ulcers

96 Pills (Approx.)

Product of USA

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1167-12020-01-31C16284748780-19d75b9d0-6d36-f424-e053-dadaa90a57ce196a3be4-9c43-7220-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1167-1Natrum sulphuricum 30C96 in 1 BOTTLEPELLET961

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1167NATRUM SULPHURICUM 30C (NATRUM SULPHURICUM) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]1Legacy NDC, 1 package rows20160608_196a3be4-9c43-7220-e054-00144ff8d46c.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
69152-116769152-1167-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM SULFATE0YPR65R21JACTIB
SUCROSEC151H8M554IACT
LACTOSEJ2B2A4N98GIACT

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
196a3be4-9c44-7220-e054-00144ff8d46c196a3be4-9c43-7220-e054-00144ff8d46c2015-06-26WarningsExact identifier
spl id: 196a3be4-9c44-7220-e054-00144ff8d46c
spl set id: 196a3be4-9c43-7220-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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