Label: MAXRELIEF- arnica montana flower spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 76509-001-01 - Packager: Natures Investment Holdings Pty Ltd
- Category: HUMAN OTC DRUG LABEL
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 December 19, 2011
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient Section
- Purpose Section
- Keep Out of Reach of Children Section
- Indications & Usage Section
- Warnings Section
-
Directions Section
DIRECTIONS:
SHAKE WELL before using. Most effective when liberally applied with 4 to 6 pumps of the spray on the affected area and importantly, on the surrounding area. Lightly rub in and reapply after 30 seconds. For optimum results, repeat 4 times daily for 3 to 5 days. When the pain has subsided, use MAXRELIEF at least once each morning and evening for continued temporary relief.
Use in conjunction with MAXRELIEF cream for even greater pain relief. If symptoms persist consult a healthcare professional.
- Inactive Ingredient Section
- Money Back Guarantee Section
- Label Information Section
-
INGREDIENTS AND APPEARANCE
MAXRELIEF
arnica montana flower sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76509-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ) ARNICA MONTANA FLOWER 50 mg in 120 mL ROSEMARY OIL (UNII: 8LGU7VM393) (ROSEMARY OIL - UNII:8LGU7VM393) ROSEMARY OIL 110 mg in 120 mL EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL 6 mg in 120 mL Inactive Ingredients Ingredient Name Strength EMU OIL (UNII: 344821WD61) ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76509-001-01 120 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/2012 Labeler - Natures Investment Holdings Pty Ltd (745559703) Registrant - Natures Investment Holdings Pty Ltd (745559703) Establishment Name Address ID/FEI Business Operations Natures Investment Holdings Pty Ltd 745559703 manufacture