Kraj: Stany Zjednoczone
Język: angielski
Źródło: NLM (National Library of Medicine)
ACONITUM NAPELLUS 3X HPUS, BRYONIA ALBA 3X HPUS, BELLADONA 3X HPUS
MARCO PHARMA INTERNATIONAL LLC
ORAL
OTC DRUG
FOR TEMPORARY RELIEF OF COLD AND FLU SYMPTOMS WITH TEMPERATURE FOR TEMPORARY RELIEF OF COLD AND FLU SYMPTOMS WITH TEMPERATURE
unapproved homeopathic
ABB- ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA LIQUID MARCO PHARMA INTERNATIONAL LLC _Disclaimer: This homeopathic product has not been evaluated by the Food and Drug_ _Administration for safety or efficacy. FDA is not aware of scientific evidence to support_ _homeopathy as effective._ ---------- ABB ACTIVE INGREDIENTS ACONITUM NAPELLUS 3X HPUS BRYONIA ALBA 3X HPUS BELLADONA 3X HPUS ETHYL ALCOHOL (20% BY VOL) AND WATER FOR TEMPORARY RELIEF OF COLD AND FLU SYMPTOMS WITH TEMPERATURE WARNINGS KEEP OUT OF REACH OF CHILDREN WARNINGS IF PREGNANT OR BREAST-FEEDING, CONSULT A HEALTH PROFESSIONAL BEFORE USE WARNINGS IF SYMPTOMS PERSIST MORE THAN A FEW DAYS, CONTACT LICENSED PRACTIONER. FOR TEMPORARY RELIEF OF COLD AND FLU SYMPTOMS WITH TEMPERATURE ADULTS AND CHILDREN: DAY 1; TAKE 5 DROPS ON THE TONGUE EVERY 15 MINUTES FOR 2 HOURS. THEN TAKE 5 DROPS ONCE EVERY HOUR. DAY 2; TAKE 5 DROPS ONCE EVERY HOUR. DAY 3; TAKE 5 DROPS EVERY TWO HOURS. CONTINUE WITH 10 DROPS THREE TIMES DAILY ABB aconitum napellus, bryonia alba, belladonna liquid PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:60986-2030 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS 3 [hp_X] in 100 mL BRYONIA ALBA WHOLE (UNII: 56K0VVT47P) (BRYONIA ALBA WHOLE - UNII:56K0VVT47P) BRYONIA ALBA WHOLE 3 [hp_X] in 100 mL BELLADONNA LEAF (UNII: 6GZW20TIOI) (BELLADONNA LEAF - UNII:6GZ W20TIOI) BELLADONNA LEAF 3 [hp_X] in 100 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) PACKAGING MARKETING START MARKETING END MARCO PHARMA INTERNATIONAL LLC # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:60986- 2030-5 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/27/2015 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE unapproved homeopathic 01/22/2015 LABELE Przeczytaj cały dokument