FDA.reportPublic FDA data

Anacardium orientale 200C

Manufacturer
Paramesh Banerji Life Sciences LLC
Effective date
2016-04-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:07:48

Label at a glance#

ProductAnacardium orientale 200C
Active ingredientSEMECARPUS ANACARDIUM JUICE
Label structure9 sections

Indications and uses

Forgetfullness & memory loss

Label contents#

Full prescribing information#

DRAG FACTS: Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Anacardium orientale 200C HPUS

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sucrose, Lactose

Purpose

OTC - PURPOSE SECTION

Forgetfullness & memory loss

Uses

INDICATIONS & USAGE SECTION

Forgetfullness & memory loss

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

Anacardium orientale 200CAnacardium orientale 200C

NDC: 69152-1092-1

Anacardium orientale 200C

Homeopathic Medicine

Forgetfullness & memory loss

96 Pills (Approx.)

Product of USA

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1092-12020-01-31C16284748780-19d75b9d0-fbb0-f424-e053-dadaa90a57ce18c6f731-d4a2-09e0-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1092-1Anacardium orientale 200C96 in 1 BOTTLEPELLET962

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1092ANACARDIUM ORIENTALE 200C (ANACARDIUM ORIENTALE) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]2Legacy NDC, 1 package rows20160429_18c6f731-d4a2-09e0-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69152-109269152-1092-1

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
SEMECARPUS ANACARDIUM JUICEY0F0BU8RDUACTIB
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
319d2af1-96ff-3de8-e054-00144ff8d46c18c6f731-d4a2-09e0-e054-00144ff8d46c2016-04-29WarningsExact identifier
spl id: 319d2af1-96ff-3de8-e054-00144ff8d46c
spl set id: 18c6f731-d4a2-09e0-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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