DOLLAR GENERAL MENTHOL PAIN RELIEF GEL ROLLON- menthol gel

Dollar General Menthol Pain Relief Gel Rollon by

Drug Labeling and Warnings

Dollar General Menthol Pain Relief Gel Rollon by is a Otc medication manufactured, distributed, or labeled by Dolgencorp, LLC, Nantong Health & Beyond Hygienic Products Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Menthol 4% 

Purpose

Topical analgesic

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with:

■ simple backache

■arthritis

■strains

■bruises

■sprains

Warnings

For external use only

Flammable 

• keep away from fire or flame

When using this product

■ use only as directed.

■avoid contact with eyes or on mucous membranes

■do not apply to woundsor damaged skin

■do not apply to irritated skin or if excessive irritation develops

■do not bandage tightly or use with heating pad or device

Stop use and ask a doctor if

■ you experience pain, swelling, or blistering of the skin

■condition worsens, or if symptoms persist for more than 7 days or clear up and occur againwithin a few days

■arthritic pain persists for more than 1O days, or redness is present, or in conditions affecting children under 12 years of age

If pregnant or breast feeding

ask a health professional before use.

Keep out of reach of children and pets.

If swallowed,get medical help or contact Poison Control Center (1-800-222-1222) right away.

Directions

Adults and children 2 years of age and older:

■ ruba thin film over affected area not more than 3 to 4 times daily

Children under 2 years of age:

■ask a doctor

■ wash hands after use with cool water

Other information

Store at room temperature

Inactive Ingredients

aloe barbadensis leaf juice, amin□methyl propanol, arctium lappa extract, arnica montana flower extract, boswellia serrata extract, calendula officinalis flower extract, camellia sinensis leaf extract, camphor,carbomer,FO&C blue no.1,FD&C yellow no.5,glycerin,ilex paraguariensis leaf
extract, isapropyl alcohol, isapropyl myristate, melissa officinalisleaf extract, methyl methacrylate crosspolymer, tocopheryl acetate, water

Label

INGREDIENTS AND APPEARANCE

DOLLAR GENERAL MENTHOL PAIN RELIEF GEL ROLLON 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55910-986
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	4 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER 940 (UNII: 4Q93RCW27E)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
ARCTIUM LAPPA WHOLE (UNII: 73070DU1LA)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
BOSWELLIA SERRATA GUM (UNII: 4PW41QCO2M)
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55910-986-01	1 in 1 PACKAGE	10/01/2025
1		73 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/01/2025

Labeler - Dolgencorp, LLC (068331990)

Registrant - Dolgencorp, LLC (068331990)

Establishment
Name	Address	ID/FEI	Business Operations
Nantong Health & Beyond Hygienic Products Inc.		421280161	manufacture(55910-986)