Label: ARNICARE- arnica montana ointment
- NDC Code(s): 0220-9023-51
- Packager: Laboratoires Boiron
- 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 January 18, 2023
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- DO NOT USE
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DOSAGE & ADMINISTRATION
Apply a thin layer of Arnicare Ointment to affected area and massage gently as soon as possible after minor injury. Repeat 3 times a day or as needed.
Apply a thin layer of Arnicare Ointment to affected area as soon as possible after minor injury. Repeat 3 times a day or as needed. If heat or ice is applied, wait 5 minutes before applying Arnicare Ointment.
- INACTIVE INGREDIENT
- HOW SUPPLIED
- PURPOSE
- STORAGE AND HANDLING
- QUESTIONS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
- WHEN USING
- DRUG INTERACTIONS
- WARNINGS
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SPL UNCLASSIFIED SECTION
ɨ Homeopathic mother tincture made from Arnica montana fresh whole plant.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ARNICARE
arnica montana ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-9023 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 1 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0220-9023-51 30 g in 1 BOX; Type 0: Not a Combination Product 06/02/2007 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/02/2007 Labeler - Laboratoires Boiron (282560473) Registrant - Boiron Inc. (014892269) Establishment Name Address ID/FEI Business Operations Boiron 282560473 manufacture(0220-9023)