Country: United States
Language: English
Source: NLM (National Library of Medicine)
ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX), SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)
Uriel Pharmacy Inc.
ECHINACEA, UNSPECIFIED
ECHINACEA, UNSPECIFIED 2 [hp_X]
ORAL
OTC DRUG
Directions: FOR ORAL USE ONLY Use: Temporary relief of headache.
unapproved homeopathic
ECHINACEA ARGENTUM- ECHINACEA ARGENTUM PELLET 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._ ---------- ECHINACEA ARGENTUM Directions: FOR ORAL USE ONLY Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2- 11: 5 pellets. Under age 2: Consult a doctor. Active Ingredients: Echinacea (Purple coneflower) 2X, Argentum met. (Silver) 30X Inactive Ingredient: Organic sucrose prepared using rhythmical processes Use: Temporary relief of headache. KEEP OUT OF REACH OF CHILDREN. Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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 Uriel, East Troy, WI 53120 shopuriel.com Lot: ECHINACEA ARGENTUM echinacea argentum pellet PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:48951-4015 ROUTE OF ADMINISTRATION ORAL Uriel Pharmacy Inc. ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX) ECHINACEA, UNSPECIFIED 2 [hp_X] SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 30 [hp_X] INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH SUCROSE (UNII: C151H8M554) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:48951- 4015-2 1350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/01/2009 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE unapproved homeopathic 09/01/2009 LABELER - Ur Read the complete document