Страна: США
мова: англійська
Джерело: NLM (National Library of Medicine)
CROTALUS HORRIDUS
Washington Homeopathic Products
ORAL
OTC DRUG
To relieve the symptoms of lightheadedness. Indications: CROTALUS HOR Lightheadedness If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.
unapproved homeopathic
CROTALUS HORRIDUS- CROTALUS HORRIDUS HORRIDUS VENOM LIQUID WASHINGTON HOMEOPATHIC PRODUCTS _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._ ---------- DRUG FACTS ACTIVE INGREDIENTS CROTALUS HORRIDUS USES To relieve the symptoms of lightheadedness. KEEP OUT OF REACH OF CHILDREN Keep this and all medicines out of reach of children. INDICATIONS Indications: CROTALUS HOR Lightheadedness STOP USE AND ASK DOCTOR If symptoms persist/worsen or if pregnant/nursing, consult your practitioner. DIRECTIONS Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner. INACTIVE INGREDIENTS Sucrose/Lactose PRINCIPAL DISPLAY PANEL The OTC potency range of CROTALUS HORRIDUS is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM. Availability is subject to change. All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled. ‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice. Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml. CROTALUS HORRIDUS crotalus horridus horridus venom liquid PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:719 19 -235 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH CRO TALUS HO RRIDUS HO RRIDUS VENO M (UNII: YHA2XLJ9 56 ) (CROTALUS HORRIDUS HORRIDUS VENOM - UNII:YHA2XLJ9 56 ) CROTALUS HORRIDUS HORRIDUS VENOM 30 [hp_C] in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH ALCO HO L (UNII: 3K9 9 58 V9 0 M) WATER (UNII: 0 59 QF0 KO0 R) PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:719 19 -235- 0 7 15 mL in 1 VIAL, GLASS; Type 0 : No t a Co mbinatio n Pro duct 0 5/17/20 11 2 NDC:719 19 -235- 0 8 3 Прочитайте повний документ