Label: ADVANCED ARNICA- natural medicine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 57955-5984-2 - Packager: King Bio 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 October 8, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Inactive Ingredients
- Dosage and Administration
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Purpose
HPUS active ingredients Purpose
Equal volumes of each ingredient in 6X, 30X, 6C, 30C, and LM1 potencies.
Arnica montana.......................................traumatic injury, sprains, bruises, body aches, muscle pain, inflammation
Arnica montana radix..............................redness and swelling, sensitivity to touch
Reference image of arnica.jpg
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Indications and Usage
Uses temporarily relieves symptoms due to injury or overexertion:
- bruises
- muscle pain
- inflammation
- body aches
- sprains
- traumatic injury
- redness and swelling
- soreness after exercise
- rheumatic pain
as per various homeopathic Materia Medicas.
King Bio Inc.
3 Westside Drive
Asheville, NC 28806
www.kingbio.com
Reference image of arnica.jpg - Warnings
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ADVANCED ARNICA
natural medicine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57955-5984 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 6 [hp_X] in 59 mL ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327) ARNICA MONTANA ROOT 6 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength ARNICA CHAMISSONIS FLOWER (UNII: 88WK5I8R3L) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57955-5984-2 1 in 1 CARTON 09/27/2011 1 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/27/2011 Labeler - King Bio Inc. (617901350) Registrant - King Bio Inc. (617901350) Establishment Name Address ID/FEI Business Operations King Bio Inc. 617901350 manufacture(57955-5984)
