Label: ARGENTUM NITRICUM 4X liquid
- NDC Code(s): 48951-1317-1
- Packager: Uriel Pharmacy Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Updated June 10, 2019
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- 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.
REFRIGERATE AFTER OPENING. USE WITHIN 30 DAYS OF OPENING.
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
ARGENTUM NITRICUM 4X
argentum nitricum 4x liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-1317 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 4 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM BICARBONATE (UNII: 8MDF5V39QO) ROSE OIL (UNII: WUB68Y35M7) POTASSIUM NITRATE (UNII: RU45X2JN0Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-1317-1 1 in 1 BAG 09/01/2009 1 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2009 Labeler - Uriel Pharmacy Inc. (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy Inc. 043471163 manufacture(48951-1317)