Label: PURPLE CONEFLOWER spray
- NDC Code(s): 48951-8318-2
- 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 July 24, 2017
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- Official Label (Printer Friendly)
- Purpose
- Dosage & Administration
- OTC-Active Ingredient
- Uses: Temporary relieves symptoms of sore throat and mouth inflammation.
- Inactive Ingredient
- Keep out of reach of children
- WARNINGS
- Ask doctor section
- Pregnancy or breast feeding section
- Questions section
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
PURPLE CONEFLOWER
purple coneflower sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-8318 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J) SAGE 1 [hp_X] CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X] ECHINACEA PALLIDA (UNII: 904CK3270L) (ECHINACEA PALLIDA - UNII:904CK3270L) ECHINACEA PALLIDA 1 [hp_X] EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 1 [hp_X] MERCURIC CYANIDE (UNII: RWG7BD1032) (MERCURIC CYANIDE - UNII:RWG7BD1032) MERCURIC CYANIDE 8 [hp_X] SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 20 [hp_X] ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 20 [hp_X] SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 20 [hp_X] Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) EUCALYPTUS OIL (UNII: 2R04ONI662) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-8318-2 360 in 1 BOTTLE, SPRAY; 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(48951-8318)