FDA.reportPublic FDA data

24-7 Relief & Recovery Pain Relieving Cream

Manufacturer
Triplicare Inc | Pure Source, LLC
Effective date
2026-04-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:55:55

Label at a glance#

Product24 7 Relief and Recovery Pain Relieving
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure9 sections

Indications and uses

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

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Menthol USP 3.7%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

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

Warnings:

WARNINGS SECTION

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

When using this product:

OTC - WHEN USING SECTION

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:

OTC - STOP USE SECTION

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

If pregnant or breast-feeding:

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

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:

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

— Info@247paincream.com

Package Labeling: 118 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling: 946 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1655936menthol 3.7 % Topical CreamPSN1
1655936menthol 37 MG/ML Topical CreamSCD1
1655936menthol 3.7 % Topical CreamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
5e18e798-5614-cf5c-0185-38b1cb77a093Product name220160822

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87656-964-0424 7 Relief and Recovery Pain Relieving118 mL in 1 TUBECREAM1181
87656-964-3224 7 Relief and Recovery Pain Relieving946 mL in 1 BOTTLECREAM9461

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87656-96487656-964-04, 87656-964-32

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
INDIAN FRANKINCENSE4PW41QCO2MIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
EDETIC ACID9G34HU7RV0IACT
GLUCOSAMINE SULFATE1FW7WLR731IACT
ILEX PARAGUARIENSIS LEAF1Q953B4O4FIACT
ISOPROPYL ALCOHOLND2M416302IACT
TEA TREE OILVIF565UC2GIACT
PYRIDOXINE HYDROCHLORIDE68Y4CF58BVIACT
POLYSORBATE 207T1F30V5YHIACT
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
TROLAMINE9O3K93S3TKIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
24 7 Relief and Recovery Pain RelievingMENTHOL, UNSPECIFIED FORMTriplicare Inc53ca807b-3ec2-4b5e-aa5a-6dcb756bb4232026-04-30WarningsExact identifier
ndc (package): 87656-964-04
ndc (package): 87656-964-32
ndc (product): 87656-964
ndc11 (package): 87656096432
ndc11 (package): 87656096404
spl id: 50acffaf-7b87-df5e-e063-6394a90ad6b5
spl set id: 53ca807b-3ec2-4b5e-aa5a-6dcb756bb423

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.