24 7 RELIEF AND RECOVERY PAIN RELIEVING- menthol, unspecified form cream

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active Ingredients:

Menthol USP 3.7%

Purpose

Topical Analgesic

Uses:

Temporary relief from minor aches and pains of sore muscles & joints associated with arthritis, simple backache, strains, bruises & sprains.

Warnings:

For external use only.Use only as directed. Keep away from excessive heat or flame.

When using this product:

Avoid contact with the eyes or mucous membranes. Do not apply to wounds or damaged skin. Do not use with other ointments, creams, sprays or liniments. Do not apply to irritated skin or if excessive irritation develops. Do not bandage. Do not use with heating pad or device. Wash hands after use with cool water.

Stop use and ask doctor if:

Condition worsens, or if symptoms persist for more than 7 days, or clear up and return.

If pregnant or breast-feeding:

Ask a health professional before use.

Keep out of the reach of children.

If accidentally ingested, get medical help or contact Poison Control Center immediately.

Directions:

Adults and children 12 years of age and older:Apply and massage on to affected areas. Repeat as needed no more than 4 times daily. Wash hands after use with cool water.

• Children under 12 years of age:Consult physician.

Other Information:

Store in a cool, dry place. Close cap tightly.

Inactive Ingredients:

Aloe Barbadensis Leaf Extract, Arnica Montana, Flower Extract, Boswellia Serrata Extract, Carbomer, Dimethyl Sulfone (MSM), EDTA, Glucosamine Sulfate, Ilex Paraguariensis Leaf Extract, Isopropyl Alcohol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Pyridoxine HCl (Vitamin B6), Phenoxyethanol/Caprylyl Glycol/Sorbic Acid, Pinus Pinaster (bark extract), Polysorbate 20, Purified Water, Tocopheryl (Vitamin E) Acetate, Triethanolamine

Questions or Comments

— Info@247paincream.com

Package Labeling: 118 mL

Package Labeling: 946 mL

INGREDIENTS AND APPEARANCE

24 7 RELIEF AND RECOVERY PAIN RELIEVING 
menthol, unspecified form cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87656-964
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	37 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
EDETIC ACID (UNII: 9G34HU7RV0)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TEA TREE OIL (UNII: VIF565UC2G)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87656-964-04	118 mL in 1 TUBE; Type 0: Not a Combination Product	04/13/2026
2	NDC: 87656-964-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/13/2026

Labeler - Triplicare Inc (057056853)

Registrant - Pure Source, LLC (080354456)