UTOM 40 NUMBER 36- sepia, conium maculatum, thuja occidentalis pellet

Utom 40 Number 36 by

Drug Labeling and Warnings

Utom 40 Number 36 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

Conium Maculatum 3C HPUS, Sepia 200C HPUS, Thuja Occidentalis 200C HPUS

Inactive Ingredients

Sucrose, Lactose

Purpose

Clears warts on skin

Uses

Clears warts 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.

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: 69152-0036-1

Utom 40

Number 36

Homeopathic Medicine

Clears warts on skin

96 Pills (Approx.)

Product of USA

INGREDIENTS AND APPEARANCE

UTOM 40 NUMBER 36 
sepia, conium maculatum, thuja occidentalis pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69152-0036
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2)	SEPIA OFFICINALIS JUICE	200 [hp_C]
CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (CONIUM MACULATUM FLOWERING TOP - UNII:Q28R5GF371)	CONIUM MACULATUM FLOWERING TOP	3 [hp_C]
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	200 [hp_C]

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

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: 69152-0036-1	96 in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/31/2014

Labeler - Paramesh Banerji Life Sciences LLC (079393726)

Establishment
Name	Address	ID/FEI	Business Operations
Paramesh Banerji Life Sciences LLC		079393726	manufacture(69152-0036) , pack(69152-0036) , label(69152-0036)