Pajjiż: Stati Uniti
Lingwa: Ingliż
Sors: NLM (National Library of Medicine)
REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ) (REHMANNIA GLUTINOSA ROOT - UNII:1BEM3U6LQQ)
HAMABIO Co., Ltd.
REHMANNIA GLUTINOSA ROOT
REHMANNIA GLUTINOSA ROOT 5 g in 100 g
ORAL
OTC DRUG
Medicine for intractable skin disease. (e.g. Psoriasis, Atopy, Eczema, Dyshidrotic eczema, Acne, Hives, Seborrheic dermatitis, Leucoplakia, etc) intake 2 spoons (under the age 10, spoon) 2~3 times daily before or after a meal
unapproved drug other
CHUN-SHIM HAEDOKSAN - REHMANNIA GLUTINOSA ROOT POWDER HAMABIO CO., LTD. _Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been_ _approved by FDA. For further information about unapproved drugs, click here._ ---------- DRUG FACTS REHMANNIA GLUTINOSA ROOT poris cocos, alisma canaliculatum, gypsum, anemarrhena asphodeloides, ostericum koreanum, aralia continentalis, schizonepeta tenuifolia, saposhnikovia divaricata, forsythia viridissima, lonicera japonica, arctium lappa Medicine for intractable skin disease. (e.g. Psoriasis, Atopy, Eczema, Dyshidrotic eczema, Acne, Hives, Seborrheic dermatitis, Leucoplakia, etc) keep out or reach of the children intake 2 spoons (under the age 10, spoon) 2~3 times daily before or after a meal 1) avoid direct sun exposure, keep it refrigerated or in cooler places 2) gently tap on the packaging a few times before intake for oral use only HAMABIO Co., Ltd. CHUN-SHIM HAEDOKSAN rehmannia glutinosa root powder PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:6 9 245-10 0 1 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH REHMANNIA GLUTINO SA RO O T (UNII: 1BEM3U6 LQQ) (REHMANNIA GLUTINOSA ROOT - UNII:1BEM3U6 LQQ) REHMANNIA GLUTINOSA ROOT 5 g in 10 0 g INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH SAPO SHNIKO VIA DIVARICATA RO O T (UNII: 8 H8 4LFK2QD) FU LING (UNII: XH37TWY5O4) PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:6 9 245-10 0 1-1 30 0 g in 1 BOTTLE MARKETING INFORMATION MARKE TING CATE GORY APPLICATION NUMBE R OR MONOGRAPH CITATION MARKE TING START DATE MARKE TING END DATE unappro ved drug o ther 0 7/0 8 /20 13 LABELER - HAMABIO Co., Ltd. (690257191) REGISTRANT - HAMABIO Co., Ltd. (690257191) ESTABLISHMENT NAME AD D RE S S ID/FEI BUSINE SS OPE RATIONS HAMABIO Co ., Ltd. 6 9 0 25719 1 ma nufa c ture (6 9 245-10 0 1) Revised: 10/2014 Aqra d-dokument sħiħ