BONE CARE- atractylodes lancea root tablet

Bone Care by

Drug Labeling and Warnings

Bone Care by is a Otc medication manufactured, distributed, or labeled by Evercarepharm Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

active ingredient: atractylodis rhizoma

INACTIVE INGREDIENT

inactive ingredient: siberian chrysanthemum, puerariae radix, rehmanniae radix et rhizoma preparata, kalopnacis cortex, zanthoxyli fructus, acanthopanax root bark, achyranthis radix, phellinus linteus teng

PURPOSE

helpful for the treatment of neuralgia, rheumatoid arthritis, thyroid, sciatica

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

take 3 times a day after meals with warm water

WARNINGS

keep in a dry, cool place
keep away from direct sunlight

DOSAGE & ADMINISTRATION

do not take if you are pregnant

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BONE CARE 
atractylodes lancea root tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42469-1001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O) (ATRACTYLODES LANCEA ROOT - UNII:CAZ6282J2O)	ATRACTYLODES LANCEA ROOT	170 mg

Inactive Ingredients
Ingredient Name	Strength
PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)
REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
KALOPANAX SEPTEMLOBUS BARK (UNII: 3PC02N4V3V)
ZANTHOXYLUM SCHINIFOLIUM WHOLE (UNII: M8QGZ6O788)
ELEUTHEROCOCCUS SESSILIFLORUS WHOLE (UNII: 1LJK2AXF5I)
ACHYRANTHES JAPONICA WHOLE (UNII: F6490528HU)
PHELLINUS LINTEUS WHOLE (UNII: YVO92B1UCA)

Product Characteristics
Color	white (white)	Score	no score
Shape	OVAL (tablet)	Size	20mm
Flavor		Imprint Code	3;hp;x
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42469-1001-1	90 in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/04/2012

Labeler - Evercarepharm Co., Ltd (557812798)

Registrant - Evercarepharm Co., Ltd (557812798)

Establishment
Name	Address	ID/FEI	Business Operations
Evercarepharm Co., Ltd		557812798	manufacture