Label: MYRISTICA ARGENTUM liquid
- NDC Code(s): 48951-7062-1
- 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.
Drug Label Information
Updated March 8, 2024
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INGREDIENTS AND APPEARANCE
MYRISTICA ARGENTUM
myristica argentum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-7062 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOS TAURUS NASAL MUCOSA (UNII: 343455G79K) (BOS TAURUS NASAL MUCOSA - UNII:343455G79K) BOS TAURUS NASAL MUCOSA 7 [hp_X] in 1 mL SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 20 [hp_X] in 1 mL VIROLA SEBIFERA RESIN (UNII: GHJ5XX5SGS) (VIROLA SEBIFERA RESIN - UNII:GHJ5XX5SGS) VIROLA SEBIFERA RESIN 4 [hp_X] in 1 mL DICHROMATE ION (UNII: 9LKY4BFN2V) (DICHROMATE ION - UNII:9LKY4BFN2V) DICHROMATE ION 6 [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:48951-7062-1 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 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(48951-7062)