Label: ARNICA RELIEF- arnica montana 10x, 30x, 100x pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 60512-9058-1 - Packager: HOMEOLAB USA 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 November 5, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS HPUS
- REFERENCES
- PURPOSE
- USES
- WARNINGS
- ASK DOCTOR
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- CARTON
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INGREDIENTS AND APPEARANCE
ARNICA RELIEF
arnica montana 10x, 30x, 100x pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-9058 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 10 [hp_X] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white Score no score Shape ROUND Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60512-9058-1 80 in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/18/2013 Labeler - HOMEOLAB USA INC. (202032533) Establishment Name Address ID/FEI Business Operations HOMEOLAB USA INC. 202032533 manufacture(60512-9058)