DAKOTA MUSCLE RELIEF ROLL-ON- menthol, unspecified form solution 
LaShe Naturals, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Dakota Muscle Relief Roll-On

Drug Facts

Active Ingredients

Menthol 6.0%

Purpose

Topical Analgesic

Uses

For the temporary relief of minor aches and pains associated with

Warnings

For external use only. Avoid contact with eyes. If contact occurs, flush eyes with water immediately.

Flammable

Keep away from fire or flame.

When using this product:

  • Use only as directed
  • Do not bandage or use with a heating pad
  • Do not apply to wounds or damaged skin
  • Discontinue use if irritation develops.

Stop use and ask your doctor if:

Condition worsens or if symptoms persist more than 7 days

  • redness is present
  • excessive irritation of the skin develops.

If pregnant or breast feeding, ask a health professional before use.

Keep out of reach of children, if ingested get medical help immediately.

Directions

Adults / Children 12 years or older:

Inactive Ingredients

Clove Bud, Emu Oil, Eucalyptus Oil, Isopropyl Alcohol, Peppermint Oil, Water, White Camphor

Distributed by:
LaShe Naturals, LLC
405 West Main, Suite 5D, West Fargo, ND 58078

PRINCIPAL DISPLAY PANEL - 90 ml Bottle Label

Dakota
MUSCLE RELIEF

FAST ALL NATURAL PAIN RELIEF

Temporary Relief From:

FAST ACTING • NOT GREASY
PLEASANT SCENT

Roll-On Muscle Relief
3oz. (90ml.)

PRINCIPAL DISPLAY PANEL - 90 ml Bottle Label
DAKOTA MUSCLE RELIEF ROLL-ON 
menthol, unspecified form solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71680-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM60 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
Water (UNII: 059QF0KO0R)  
Peppermint Oil (UNII: AV092KU4JH)  
Eucalyptus Oil (UNII: 2R04ONI662)  
Camphor Oil, White (UNII: 26P3H26Z9X)  
CLOVE OIL (UNII: 578389D6D0)  
Emu Oil (UNII: 344821WD61)  
Xanthan Gum (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71680-002-0390 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product09/19/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34811/01/2011
Labeler - LaShe Naturals, LLC (053397499)

Revised: 12/2021
Document Id: 143397ce-e7b9-4eb2-8fa2-6b2ce8f088af
Set id: 880d39d5-63ba-42c2-996a-78b835550524
Version: 3
Effective Time: 20211208
 
LaShe Naturals, LLC