MENTHOL PAIN RELIEVING GEL- pain relieving gel gel

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active Ingredient- Methanol 2 %

Purpose- External Pain Reliever

Uses

Temporary relief of minor pains of muscle and joints associated with

• simple backache
• arthritis
• sprains, strains or bruises

Warnings

For External Use Only.

Avoid Contact with eyes.

Do not Use

Internally
with heating pads or devices
on wound or damaged skin

Ask a doctor before use

if have sensitive skin

Stop Use and Ask a Doctor if

condition worses

symptoms last more than 7 days, oe clear up and occur again within a few days

redness or irritaion develops

When Using this Product

Use Only as Directed

do not bandage tightly

Avoid contact within eyes and mucos membranes

If Prgenant or Breast Feeding

Ask a healthcare professional before use

Keep Out of the Children

Incase of accidental ingestion, get medical help or contact a poison control center immediately

Directions

Adults and Childern 2 years and older

Clean skin thoroughly.

Apply liberally to affected area not more than3-4 times daily.

No Protective cover needed.

May be used with ice packs.

May be used with wet or dry bandages, but wrap loosely.

Childern under 2 years of age.

Other Information

Store 59°-86°F (15°-30°C)

Keep tightly closed

Do not use, pour, spill or store near heat or open flame.

Store 59°-86°F (15°-30°C)

Keep tightly closed

Do not use, pour, spill or store near heat or open flame.

Other Ingredients

Camphor

Carbomer

FD&C Blue #1

Isopropyl Alcohol

Propylene Glycol

Purified Water

Sodium Hydroxide

Indications

Cooling, Pain relieving gel for muscle aches

arthiritis pain

simple backache

Dosage and Administration

Menthol 2 %

Therapeutic

Greaseless

Net Wt- 8 FL OZ (227 g)

Package Label

NeilMed Menthol Pain Relieving Gel

Therapeutic

Greeseless

Cooling, pain, relieving gel for muscle aches,

arthiritis pain,

Simple backache

INGREDIENTS AND APPEARANCE

MENTHOL PAIN RELIEVING GEL 
pain relieving gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 13709-357
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	4.54 g  in 227 g

Inactive Ingredients
Ingredient Name	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
CARBOMER (UNII: 0A5MM307FC)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13709-357-01	1 in 1 CARTON	05/07/2026
1		227 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	05/07/2026

Labeler - NeilMed Pharmaceuticals Inc (799295915)

Establishment
Name	Address	ID/FEI	Business Operations
NeilMed Pharmaceuticals Inc		799295915	manufacture(13709-357)