MENTHOL- menthol gel 
SUNSET PAIN RELIEF ROLL-ON 3OZ

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72937-004-03

Menthol 4%

Topical Analgesic

USE

Aid for temporary local relief of minor pain in muscles or joints.

For external use only. · Ask a doctor before use if you have redness over affected area

Use only as directed.
Do not bandage tightly or use with a heating pad.
Avoid contact with eyes and mucous membranes.
Do not apply to wounds or damaged, broken or irritated skin.
If you experience an allergic reaction, discontinue use and consult a doctor.

Do not expose the area treated with product to heat or direct sunlight.

Stop use and ask a doctor if

Condition worsens.
Redness is present.
Irritation develops.
Symptoms persist for more than 7 days or clear up occur again within a few days.

You experience signs injury, such as pain, swelling or blistering where the product was applied.

Ask a health professional before use.

If swallowed, get medical help, or contact a Poison Control Center right away.

DIRECTIONS

Adults and Children over 12 years

Apply a small amount to the affected area.
Massage in circular motion, let set for a few seconds.
Repeat as necessary, but no more than 3 to 4 times daily.

Children under 12 years of age: do not use, consult a doctor.

Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

Water (Aqua), Alcohol Denat, Glycerin, Ceteareth-25, Caprylic/Capric Triglyceride, Calendula Officinalis Extract, Benzyl Alcohol, Salicylic Acid, Sorbic Acid, Sodium Hydroxide, Carbomer, Cannabidiol, Methyl Salicylate.

SUNSET PAIN RELIEF +350 CBD ROLL-ON

sunset roll on gold

MENTHOL 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72937-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
CANNABIDIOL (UNII: 19GBJ60SN5)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
SORBIC ACID (UNII: X045WJ989B)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72937-004-0390 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product09/24/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01709/24/2019
Labeler - SUNSET PAIN RELIEF ROLL-ON 3OZ (067218145)

Revised: 1/2024
Document Id: 06e902ac-e32e-43f1-e063-6294a90a4328
Set id: 934d4638-b47b-187d-e053-2995a90ae69d
Version: 3
Effective Time: 20240126
 
SUNSET PAIN RELIEF ROLL-ON 3OZ