Arnica Carbo Special Order

Arnica Carbo Special Order

Drug Labeling and Warnings

Drug Details

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ARNICA CARBO SPECIAL ORDER- arnica carbo special order liquid 
Uriel Pharmacy Inc.

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.

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Arnica Carbo Special Order

Directions: FOR ORAL USE.

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

Active Ingredients: Arnica e rad. 6X, Atropa belladonna e pl. tota 6X, Melilotus ex herba 8X, Carbo Betulae 10X, Lachesis e veneno 12X

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.

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

PRODUCT LABEL

ARNICA CARBO SPECIAL ORDER 
arnica carbo special order liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 48951-1231
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327) ARNICA MONTANA ROOT6 [hp_X]  in 1 mL
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA6 [hp_X]  in 1 mL
MELILOTUS INDICUS SEED (UNII: F22I9R6Q0X) (MELILOTUS INDICUS SEED - UNII:F22I9R6Q0X) MELILOTUS INDICUS SEED8 [hp_X]  in 1 mL
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL10 [hp_X]  in 1 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM12 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 48951-1231-110 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(48951-1231)

Revised: 9/2014
 
Uriel Pharmacy Inc.


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