Label: ARGENTUM NITRICUM tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 15631-0520-0, 15631-0520-1, 15631-0520-2, 15631-0520-3, view more15631-0520-4, 15631-0520-5, 15631-0520-6, 15631-0520-7 - Packager: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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 Label Information
Updated December 30, 2015
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- ACTIVE INGREDIENT
- USES
- INDICATIONS
- DOSAGE
- WARNINGS
- INACTIVE INGREDIENTS
- STORAGE
- QUESTIONS OR COMMENTS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ARGENTUM NITRICUM
argentum nitricum tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:15631-0520 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 6 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:15631-0520-0 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:15631-0520-1 4 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:15631-0520-2 50 in 1 CONTAINER; Type 0: Not a Combination Product 4 NDC:15631-0520-3 100 in 1 CONTAINER; Type 0: Not a Combination Product 5 NDC:15631-0520-4 250 in 1 CONTAINER; Type 0: Not a Combination Product 6 NDC:15631-0520-5 500 in 1 CONTAINER; Type 0: Not a Combination Product 7 NDC:15631-0520-6 1000 in 1 CONTAINER; Type 0: Not a Combination Product 8 NDC:15631-0520-7 10000 in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/30/2015 Labeler - Rxhomeo Private Limited d.b.a. Rxhomeo, Inc (650833994) Establishment Name Address ID/FEI Business Operations Rxhomeo, Inc 832534981 wholesale drug distributor(15631-0520) Establishment Name Address ID/FEI Business Operations Rxhomeo Private Limited d.b.a. Rxhomeo, Inc 650833994 manufacture(15631-0520) , label(15631-0520)