BATINHA 40 (NUMBER 532)- hypericum peltatum, arsenicum album pellet

Batinha 40 (Number 532) by

Drug Labeling and Warnings

Batinha 40 (Number 532) 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

Hypericum perforatum 30C HPUS, Kalmia latifolia 6C HPUS

Inactive Ingredients

Sucrose, Lactose

Purpose

Relieves acute arthritic pains throughout the body

Uses

Relieves acute arthritic pains throughout the body

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: 69152-0532-1

Batinha 40

Number 532

Homeopathic Medicine

Relieves acute arthritic pains throughout the body

96 Pills (Approx.)

Product of USA

INGREDIENTS AND APPEARANCE

BATINHA 40 (NUMBER 532) 
hypericum peltatum, arsenicum album pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69152-0532
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	30 [hp_C]
KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (KALMIA LATIFOLIA LEAF - UNII:79N6542N18)	KALMIA LATIFOLIA LEAF	6 [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: 69152-0532-1	96 in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2018

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

Labeler - Paramesh Banerji Life Sciences LLC (079393726)

Establishment
Name	Address	ID/FEI	Business Operations
Paramesh Banerji Life Sciences LLC		079393726	pack(69152-0532) , manufacture(69152-0532) , label(69152-0532)