ARNICA RELIEF- arnica montana cream 
Homeocare Laboratories

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.

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Arnica Relief Cream

Active Ingredients:

Arnica Montana 1x (HPUS) 7%

Purpose:

As a topical aid for the relief of bruising, injuries, muscle aches, pain relief and pre-post surgically.

Keep out of the reach of children.

Keep out of the reach of children.

Indications for Usage:

As a topical aid for the relief of bruising, injuries, muscle aches, pain relief and pre-post surgically.

Warnings:

For external use only. Ask a doctor before use if pregnant or breastfeeding. Keep out of the reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredients:

Avocado Oil, Caprylyl Glycol, Cetyl Alcohol, Dimethicone, Dimethyl Taurate Copolymer, Glycerin USP, Glyceryl Stearate, Caprylic/Capric Triglyceride, Hexylen Glycol, Phenoxyethanol, Polyethylene, Sodium Polyacrylate, Potassium Sorbate, Purified Water, Sodium Acrylate/Sodium Acryloyl, Sunflower Oil.

Dosage & Administration:

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 years old (under 2 years ask a doctor).

Arnica Relief Cream

Arnica Cream Front Pic.jpgArnica Cream Back Pic.jpg

ARNICA RELIEF 
arnica montana cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61727-112
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA1 [hp_X]  in 56.7 g
Inactive Ingredients
Ingredient NameStrength
AVOCADO OIL (UNII: 6VNO72PFC1)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
TRICAPRIN (UNII: O1PB8EU98M)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61727-112-0256.7 g in 1 TUBE; Type 0: Not a Combination Product12/21/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic04/10/2012
Labeler - Homeocare Laboratories (088248828)
Registrant - Homeocare Laboratories (088248828)
Establishment
NameAddressID/FEIBusiness Operations
Homeocare Laboratories088248828manufacture(61727-112)

Revised: 12/2018
Document Id: 7d8df6df-1805-fd19-e053-2a91aa0a1e52
Set id: 28a8e33e-cfae-4837-8b76-1bced9d70045
Version: 2
Effective Time: 20181221
 
Homeocare Laboratories