Bufo rana 200C

Manufacturer: Paramesh Banerji Life Sciences LLC
Effective date: 2017-02-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:08:31

Label at a glance#

ProductBufo rana 200C

Active ingredientBUFO BUFO CUTANEOUS GLAND

Label structure9 sections

Indications and uses

Severe pain in ulcers

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact+1-732-743-5936

Websitewww.pblifesciences.com

www.pblifesciences.com/permapotent

Label contents#

Full prescribing information#

DRUG FACTS: Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Bufo rana 200C HPUS

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sucrose, Lactose

Purpose

OTC - PURPOSE SECTION

Severe pain in ulcers

Uses

INDICATIONS & USAGE SECTION

Severe pain in 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 Poison Control Center (1-800-222-1222).

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

Bufo rana 200C

NDC: 69152-1097-1

Bufo rana 200C

Homeopathic Medicine

Severe pain in ulcers

96 Pills (Approx.)

Product of USA

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69152-1097-1	2020-01-31	C162847	48780-1	9d75b9d0-9d87-f424-e053-dadaa90a57ce	4787a538-8600-5f51-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69152-1097-1	Bufo rana 200C	96 in 1 BOTTLE	PELLET	96		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69152-1097	BUFO RANA 200C (BUFO RANA) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]	1	Legacy NDC, 1 package rows	20170202_4787a538-8600-5f51-e054-00144ff8d46c.zip

Products#

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

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

Bufo rana 200C
Bufo rana
SUCROSE
LACTOSE, UNSPECIFIED FORM
BUFO BUFO CUTANEOUS GLAND

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69152-1097	69152-1097-1

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
Name	UNII	Kind
SUCROSE	C151H8M554	IACT
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	IACT
BUFO BUFO CUTANEOUS GLAND	Q59QU6N72Q	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
4787a538-8601-5f51-e054-00144ff8d46c			4787a538-8600-5f51-e054-00144ff8d46c	2017-02-02	Warnings	Exact identifier spl id: 4787a538-8601-5f51-e054-00144ff8d46c spl set id: 4787a538-8600-5f51-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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