Label: AQUILINUM TARAXACUM AMPULES liquid
- NDC Code(s): 48951-1285-1
- Packager: Uriel Pharmacy 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 May 2, 2018
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- DOSAGE & ADMINISTRATION
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INGREDIENTS AND APPEARANCE
AQUILINUM TARAXACUM AMPULES
aquilinum taraxacum ampules liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-1285 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X) (DRYOPTERIS FILIX-MAS ROOT - UNII:C0ZK0RRF5X) DRYOPTERIS FILIX-MAS ROOT 5 [hp_X] in 1 mL PTERIDIUM AQUILINUM WHOLE (UNII: 05T3M06HCM) (PTERIDIUM AQUILINUM WHOLE - UNII:05T3M06HCM) PTERIDIUM AQUILINUM WHOLE 5 [hp_X] in 1 mL CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN) CHELIDONIUM MAJUS 5 [hp_X] in 1 mL TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C) (TARAXACUM PALUSTRE ROOT - UNII:GCZ4W7077C) TARAXACUM PALUSTRE ROOT 5 [hp_X] in 1 mL SALIX ALBA FLOWER (UNII: 905Y746BSW) (SALIX ALBA FLOWER - UNII:905Y746BSW) SALIX ALBA FLOWER 5 [hp_X] in 1 mL SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (SOLIDAGO VIRGAUREA FLOWERING TOP - UNII:5405K23S50) SOLIDAGO VIRGAUREA FLOWERING TOP 5 [hp_X] in 1 mL SALIX PURPUREA BARK (UNII: 287VJO13M9) (SALIX PURPUREA BARK - UNII:287VJO13M9) SALIX PURPUREA BARK 5 [hp_X] in 1 mL WILLOW BARK (UNII: S883J9JDYX) (WILLOW BARK - UNII:S883J9JDYX) WILLOW BARK 5 [hp_X] in 1 mL ASPLENIUM SCOLOPENDRIUM TOP (UNII: HJA3YWQ7HL) (ASPLENIUM SCOLOPENDRIUM TOP - UNII:HJA3YWQ7HL) ASPLENIUM SCOLOPENDRIUM TOP 5 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-1285-1 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(48951-1285)