Label: ARGENTITE 6X powder
- NDC Code(s): 48951-1376-4
- 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.
Drug Label Information
Updated November 11, 2024
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains lactose. 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.
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INGREDIENTS AND APPEARANCE
ARGENTITE 6X
argentite 6x powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-1376 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER SULFIDE (UNII: 9ZB10YHC1C) (SILVER CATION - UNII:57N7B0K90A) SILVER SULFIDE 6 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-1376-4 50 g 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 - Uriel Pharmacy, Inc. (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy, Inc. 043471163 manufacture(48951-1376)
