ARNICA- arnica liquid 
Humco Holding Group, Inc.

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 Tincture

HUMCO Arnica Tincture

Drug Facts

Active Ingredient

Arnica Flowers, 20 grams per 100cc of tincture

Purpose

Soreness relief

USE:

For the temporary relief of bruises and soreness.

Warnings

When using this product

do not apply to irritated skin. Avoid getting into eyes or on mucous membranes.

Stop use and consult a doctor

if a rash or excessive irritation of the skin develops.

Keep out of reach of children.

In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. If pregnant or breastfeeding ask a health professional before use.

Directions

  • When applied as a tincture, dilute with one or two parts of Rubbing Alcohol.
  • May be added to hot water that is being used in hot packs.
  • Apply to affected area, repeat as needed.

These statements have not been evaluated by the FDA. This product is not intended to diagnose, cure, treat or prevent any disease.

Inactive Ingredient

Isopropyl Alcohol and Purified Water.

Other Information

  • Flammable: Keep away from spark, heat and flame. Store in cool dry place.

Principal Display Panel

NDC 0395-0115-94
ARNICA TINCTURE
Soreness relief
4 fl oz (118 mL)

Principal Display Panel
NDC 0395-0115-94
ARNICA TINCTURE
Soreness relief
4 fl oz (118 mL)

ARNICA 
arnica liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-0115
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ) ARNICA MONTANA FLOWER200 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0395-0115-94118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/199706/30/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/01/199706/30/2022
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc.825672884manufacture(0395-0115) , analysis(0395-0115) , pack(0395-0115) , label(0395-0115)

Revised: 2/2020
 
Humco Holding Group, Inc.