Country: United States
Language: English
Source: NLM (National Library of Medicine)
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U), BOS TAURUS NASAL MUCOSA (UNII: 343455G79K) (BOS TAURUS NASAL MUCOSA - UNII:343455G79K), SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)
Uriel Pharmacy Inc.
BERBERIS VULGARIS ROOT BARK
BERBERIS VULGARIS ROOT BARK 3 [hp_X] in 1 mL
ORAL
OTC DRUG
Directions: FOR ORAL USE. Use: Temporary relief of sinus congestion.
unapproved homeopathic
BERBERIS QUARTZ- BERBERIS QUARTZ 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._ ---------- BERBERIS QUARTZ Directions: FOR ORAL USE. Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow. Active Ingredients: Berberis (Barberry) 3X, Tunica mucosa nasi (Bovine nasal mucosa) 7X, Quartz (Rock crystal) 20X Inactive Ingredients: Water, Salt "prepared using rhythmical processes" Use: Temporary relief of sinus congestion. 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 conditons or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 shopuriel.com Lot: BERBERIS QUARTZ berberis quartz liquid PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:48951-2054 Uriel Pharmacy Inc. ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 3 [hp_X] in 1 mL BOS TAURUS NASAL MUCOSA (UNII: 343455G79K) (BOS TAURUS NASAL MUCOSA - UNII:343455G79K) BOS TAURUS NASAL MUCOSA 7 [hp_X] in 1 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 20 [hp_X] in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:48951- 2054-1 10 in 1 BOX 09/01/2009 1 1 mL in 1 AMPULE; Type 1: Convenience Kit of Co- Package MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETI Read the complete document