Label: ARGENTUM MURIATICUM pellet
- NDC Code(s): 66096-788-01
- Packager: OHM PHARMA 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.
Updated January 14, 2021
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- ACTIVE INGREDIENT
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- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
argentum muriaticum pellet
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66096-788 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER CHLORIDE (UNII: MWB0804EO7) (SILVER CATION - UNII:57N7B0K90A) SILVER CHLORIDE 6 [hp_C] in 6 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score Shape ROUND Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66096-788-01 6 [hp_C] in 1 TUBE; Type 0: Not a Combination Product 11/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/01/2019 Labeler - OHM PHARMA INC. (030572478) Establishment Name Address ID/FEI Business Operations OHM PHARMA INC. 030572478 manufacture(66096-788)