- 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. Consult a doctor before use for serious conditions or if conditons worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MYRISTICA ARGENTUM SPECIAL ORDER
myristica argentum special order liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-7144 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 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 Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-7144-3 60 mL in 1 BOTTLE, DROPPER; 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(48951-7144)