CYTOPAN 40 (NUMBER 548)- arnica montana, rhus toxicodendron pellet

Cytopan 40 (Number 548) by

Drug Labeling and Warnings

Cytopan 40 (Number 548) by is a Homeopathic medication manufactured, distributed, or labeled by Paramesh Banerji Life Sciences LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS: Active Ingredients

Arnica montana 30C HPUS, Rhus toxicodendron 200C HPUS

Inactive Ingredients

Sucrose, Lactose

Purpose

Treats low platelet count and black patches on skin

Uses

Treats low platelet count and black patches on skin

Warnings

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

Keep out of reach of children

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

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

Manufactured by

Paramesh Banerji Life Sciences, LLC.

North Brunswick, NJ 08902, USA.

Tel: +1-732-743-5936

Email: info@pblifesciences.com

Principal Display Panel

NDC: 69152-0548-1

Cytopan 40

Number 548

Homeopathic Medicine

Treats low platelet count and black patches of skin

96 Pills (Approx.)

Product of USA

INGREDIENTS AND APPEARANCE

CYTOPAN 40 (NUMBER 548) 
arnica montana, rhus toxicodendron pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69152-0548
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	30 [hp_C]
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	200 [hp_C]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	white	Score
Shape	ROUND	Size	4mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69152-0548-1	96 in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/23/2014

Labeler - Paramesh Banerji Life Sciences LLC (079393726)

Establishment
Name	Address	ID/FEI	Business Operations
Paramesh Banerji Life Sciences LLC		079393726	manufacture(69152-0548) , pack(69152-0548) , label(69152-0548)