Your browser does not support JavaScript! APIS GELSEMIUM LIQUID [URIEL PHARMACY INC.]
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APIS GELSEMIUM liquid
[Uriel Pharmacy Inc.]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL unapproved homeopathic
NOTE: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 Sections

Directions: FOR ORAL USE ONLY.

Take the contents of one ampule
under the tongue and hold for
30 seconds, then swallow.

Active Ingredients: Berberis e rad.
3X, Gelsemium e rad. 3X, Apis ex
animale 4X, Gnaphalium e pl. tota
4X, Colchicum e pl. tota 5X, Formica
ex animale 5X, Arnica e rad. 10X

Inactive Ingredients: Water, Salt

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions

or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Natural

ingredients may cause color, scent and/or taste variation.


Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com

product label

APIS GELSEMIUM 
apis gelsemium liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:48951-1057
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BERBERIS VULGARIS ROOT BARK (BERBERIS VULGARIS ROOT BARK) BERBERIS VULGARIS ROOT BARK3 [hp_X]  in 1 mL
GELSEMIUM SEMPERVIRENS ROOT (GELSEMIUM SEMPERVIRENS ROOT) GELSEMIUM SEMPERVIRENS ROOT3 [hp_X]  in 1 mL
APIS MELLIFERA (APIS MELLIFERA) APIS MELLIFERA4 [hp_X]  in 1 mL
PSEUDOGNAPHALIUM LUTEOALBUM LEAF (PSEUDOGNAPHALIUM LUTEOALBUM LEAF) PSEUDOGNAPHALIUM LUTEOALBUM LEAF4 [hp_X]  in 1 mL
COLCHICUM AUTUMNALE FLOWER (COLCHICUM AUTUMNALE FLOWER) COLCHICUM AUTUMNALE FLOWER5 [hp_X]  in 1 mL
FORMICA RUFA (FORMICA RUFA) FORMICA RUFA5 [hp_X]  in 1 mL
ARNICA MONTANA ROOT (ARNICA MONTANA ROOT) ARNICA MONTANA ROOT10 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM CHLORIDE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-1057-110 in 1 BOX
11 mL in 1 AMPULE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
NameAddressID/FEIBusiness Operations
Uriel Pharmacy Inc.043471163manufacture(48951-1057)

Revised: 3/2014
 
Uriel Pharmacy Inc.

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