Država: Združene države Amerike
Jezik: angleščina
Source: NLM (National Library of Medicine)
DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B)
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
ORAL
OTC DRUG
Swollen Legs Condition listed above or as directed by the physician
unapproved homeopathic
DIGITALIS PURPUREA- DIGITALIS PURPUREA TABLET RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC _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._ ---------- ACTIVE INGREDIENT DIGITALIS PURPUREA HPUS 6X and Higher USES Swollen Legs INDICATIONS Condition listed above or as directed by the physician DOSAGE Adults- Take 4 or 6 Tablets by mouth, three times daily or as suggested by physician. Children 2 years and older- take 1/2 the adult dose. WARNINGS This product is to be used for self-limiting conditions If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional As with any drug, if you are pregnant, or nursing a baby, seek professional advice before taking this product Keep this and all medication out of reach of children Do not use if capseal is broken or missing. Close the cap tightly after use. INACTIVE INGREDIENTS Lactose STORAGE Store in a cool dark place QUESTIONS OR COMMENTS www.Rxhomeo.com | 1.888.2796642 | info@rxhomeo.com Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758 PACKAGE LABEL.PRINCIPAL DISPLAY PANEL DIGITALIS PURPUREA digitalis purpurea tablet PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:156 31-0 573 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH DIGITALIS (UNII: F1T8 QT9 U8 B) (DIGITALIS - UNII:F1T8 QT9 U8 B) DIGITALIS 6 [hp_X] INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH LACTO SE (UNII: J2B2A4N9 8 G) PRODUCT CHARACTERISTICS COLOR white S CORE no sco re S HAP E ROUND S IZ E 3mm FLAVOR IMPRINT CODE CONTAINS PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:156 31-0 573- 0 1 in 1 BLISTER PACK; Type 0 : No t a Co mbinatio n Pro duct 2 NDC:156 31-0 573-1 4 in 1 BLISTER PACK; Type 0 : No t a Co mbinatio n Pro duct 3 NDC:156 31-0 573-2 50 in 1 CONTAINER; Type 0 : No t a Co Preberite celoten dokument