Label: BRAZMEDICS ARNICA CREAM cream
- NDC Code(s): 61727-114-02
- Packager: Homeocare Laboratories
- 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 July 6, 2018
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient:
- Purpose
- Keep out of the reach of children
- Warnings:
- Inactive Ingredients:
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Directions:
For external use only. Apply generously to affected area, 2 to 3 times daily or as needed. Rub gently until complete absorption. Safe for children over 2 year old (under 2 years ask a doctor).
When using this product: Do not get into eyes and do not apply on open skin. Stop use and ask a doctor if: Condition worsens, symptoms last more than 7 days, you are allergic to any of the ingredients.
- Directions:
- Brazmedics Arnica Front Label
- Brazmedics Arnica Cream Back Label
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INGREDIENTS AND APPEARANCE
BRAZMEDICS ARNICA CREAM
brazmedics arnica cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61727-114 Route of Administration TOPICAL 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 [hp_X] Inactive Ingredients Ingredient Name Strength AVOCADO OIL (UNII: 6VNO72PFC1) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) TRICAPRIN (UNII: O1PB8EU98M) HEXYLENE GLYCOL (UNII: KEH0A3F75J) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) GLYCERIN (UNII: PDC6A3C0OX) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CETYL ALCOHOL (UNII: 936JST6JCN) PHENOXYETHANOL (UNII: HIE492ZZ3T) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) SODIUM ACRYLATE (UNII: 7C98FKB43H) SUNFLOWER OIL (UNII: 3W1JG795YI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61727-114-02 1 [hp_X] in 1 TUBE; Type 0: Not a Combination Product 07/06/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2018 Labeler - Homeocare Laboratories (088248828) Registrant - Homeocare Laboratories (088248828) Establishment Name Address ID/FEI Business Operations Homeocare Laboratories 088248828 manufacture(61727-114)