Land: USA
Språk: engelska
Källa: NLM (National Library of Medicine)
CUPRIC ACETATE (UNII: 39M11XPH03) (CUPRIC CATION - UNII:8CBV67279L), ZINC VALERATE DIHYDRATE (UNII: MN0RX54EQA) (VALERIC ACID - UNII:GZK92PJM7B)
Uriel Pharmacy Inc.
CUPRIC ACETATE
CUPRIC ACETATE 5 [hp_X] in 1 mL
ORAL
OTC DRUG
Directions: FOR ORAL USE ONLY. Use: Temporary relief of cramps.
unapproved homeopathic
CUPRUM ACETICUM ZINCUM VALERIANICUM- CUPRUM ACETICUM ZINCUM VALERIANICUM LIQUID URIEL PHARMACY 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._ ---------- CUPRUM ACETICUM ZINCUM VALERIANICUM Directions: FOR ORAL USE ONLY. Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor. Active Ingredients: Cuprum aceticum (Copper acetate) 5X, Zincum valerianicum (Valerate of zinc) 5X Inactive Ingredients: Distilled water, Organic cane alcohol Use: Temporary relief of cramps. KEEP OUT OF REACH OF CHILDREN. Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing. Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com CUPRUM ACETICUM ZINCUM VALERIANICUM cuprum aceticum zincum valerianicum liquid PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:48 9 51-3143 ROUTE OF ADMINISTRATION ORAL Uriel Pharmacy Inc. ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH CUPRIC ACETATE (UNII: 39 M11XPH0 3) (CUPRIC CATION - UNII:8 CBV6 7279 L) CUPRIC ACETATE 5 [hp_X] in 1 mL ZINC VALERATE DIHYDRATE (UNII: MN0 RX54EQA) (VALERIC ACID - UNII:GZK9 2PJM7B) ZINC VALERATE DIHYDRATE 5 [hp_X] in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH WATER (UNII: 0 59 QF0 KO0 R) ALCO HO L (UNII: 3K9 9 58 V9 0 M) PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:48 9 51-3143- 3 6 0 mL in 1 BOTTLE, GLASS; Type 0 : No t a Co mbinatio n Pro duc t 0 9 /0 1/20 0 9 MARKETING INFORMATION MARKE TING CATE GORY APPLICATION NUMBE R OR MONOGRAPH CITATION MARKE TIN Läs hela dokumentet