FDA.reportPublic FDA data

Jointflex

Manufacturer
Strides Consumer LLC | Beltapharm SPA
Effective date
2025-04-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:58:55

Label at a glance#

ProductJointflex
Active ingredientCAMPHOR (SYNTHETIC)
Label structure14 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Dosage and administration

Rotate the massager head to ON position and squeeze tube gently to dispense. Return the massager head to OFF position. Using a circular pattern, gently massage over the pain inflicted area using the built-in roller balls until the Emulsion Gel disappears. adults and children 12 years of age and older: clean, rinse and dry skin prior to application apply generously to painful muscles and joints, gently massaging un...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor (3.2%)

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses:

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with:

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Warnings:

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • if skin is irritated or damaged
  • excessive irritation develops
  • 12 years of age or under

Ask a doctor befor use if you have

OTC - ASK DOCTOR SECTION

  • redness over the affected area

When using this product

OTC - WHEN USING SECTION

  • use only as directed
  • avoid contact with the eyes and mucous membranes
  • do not apply to wounds, damaged, broken or irritated skin
  • do not bandage tightly or use a heating pad
  • do not swallow

Stop use and ask doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days
  • redness develops

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

Rotate the massager head to ON position and squeeze tube gently to dispense. Return the massager head to OFF position. Using a circular pattern, gently massage over the pain inflicted area using the built-in roller balls until the Emulsion Gel disappears.

adults and children 12 years of age and older:
  • clean, rinse and dry skin prior to application
  • apply generously to painful muscles and joints, gently massaging until the JointFlex® Night Time Pain Relief Emulsion Gel disappears
  • repeat as necessary, but no more than 4 times a day
  • for optimum benefit, use daily for at least two weeks and continue to use daily thereafter
children under 12 years of age:
  • ask a doctor

Other information:

OTHER SAFETY INFORMATION

  • store at room temperature with the cap closed
  • notice: because this product contains natural ingredients, color may vary

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Acetylated Lanolin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Vera, C12-15 Alkyl Benzoate, Chondroitin Sulfate, Diazolidinyl Urea, Dimethicone, Dimethiconol Stearate, Disodium EDTA, dl Panthenol, Fragrance, Glucosamine Sulfate, Glycerin, Glycerol Stearate, Glycosaminoglycans, Hydroxylated Lanolin, Hydroxpropyl Methycellulose, Iodopropynyl Butylcarbamate, Methyl Gluceth-20, Methyl Glucose Sesquistearate, Peppermint Oil, Polysorbate 20, Potassium Carbomer, Purified Water, Tocopheryl Acetate (Vitamin E).

Questions or comments?

OTC - QUESTIONS SECTION

Call (866) 235-4581 or email stridesconsumer@emersongroup.com

Manufactured for

Strides Consumer LLC,

East Brunswick, NJ 08816

Licensed user of trademarks. ©2022 Strides Consumer LLC

†Results based on a 2021 Healthcare Provider survey conducted by InStep Health as part of a point-of-care marketing campaign sponsored by Strides Consumer LLC.

www.jointflex.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Flex Your FreedomTM

Visit www.jointflex.com for more information

DEEP PENETRATING Fusome ® Technology

Quick & effective penetration

Targeted pain relief

Long lasting relief when used daily

Roller-FlexTM Massager gently works to reduce pain right at the source

Roller-FlexTMMassager

Innovative Massage Applicator

#1 CLINICALLY RECOMMENDED† JOINT PAIN CREAM

Effectively Reduces Joint Pain

Immediate & Long Lasting Relief*

Relaxing** Lavender DreamScentTM

Contains Glucosamine & Chondroitin for skin conditioning

NDC 72927-976-02

NET WT 3.5 OZ (99g)

Night Time Pain Relief

Back, Neck & Shoulde

Knee & Elbow

Foot, Ankle, Leg

Hand & Wrist

*When applied as directed

**fragrance technology validated using Sandman Classifier Test

Roller-FlexTMMassager

5 Stainless steel rollerballs

Deep pressure massage applicator

Cool to the touch

Targeted pain relief

Night Time Pain Relief Emulsion Gel

TUBES ARE FILLED BY WEIGHT NOT VOLUME

011-1650C-R01

JointFlex Lavender
JointFlex Lavender

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2181415camphor 3.2 % Topical CreamPSN4
2282659Jointflex 3.2 % Topical CreamPSN4
2282659camphor 32 MG/ML Topical Cream [Jointflex]SBD4
2181415camphor 32 MG/ML Topical CreamSCD4
2181415camphor 3.2 % Topical CreamSY4
2282659Jointflex 32 MG/ML Topical CreamSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72927-976-02Jointflex1 in 1 CARTONCREAM14
72927-976-02Jointflex99 g in 1 TUBE, WITH APPLICATORCREAM994

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72927-976JOINTFLEX (CAMPHOR) CREAM [STRIDES CONSUMER LLC]4Current NDC, Legacy NDC, 2 package rows20250410_cb5ca02b-0bc1-4b0b-b4b1-abef3222aa56.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72927-97672927-976-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
ACETYLATED LANOLIN2X654GD19HIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
CARBOMER 1342809Y72KV36IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
CHONDROITIN SULFATE (SHARK)2ZAJ1K50XHIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
DIMETHICONE92RU3N3Y1OIACT
EDETATE DISODIUM7FLD91C86KIACT
GLUCOSAMINE SULFATE POTASSIUM CHLORIDE15VQ11I66NIACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
HYDROXYLATED LANOLINEOI0B9800CIACT
HYPROMELLOSES3NXW29V3WOIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
METHYL GLUCETH-20J3QD0LD11PIACT
METHYL GLUCOSE SESQUISTEARATEV1YW10H14DIACT
PANTHENOLWV9CM0O67ZIACT
PEPPERMINT OILAV092KU4JHIACT
POLYOXYL 40 STEARATE13A4J4NH9IIACT
POLYSORBATE 207T1F30V5YHIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
SHARK CARTILAGED2YCN1I522IACT
WATER059QF0KO0RIACT

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
JointflexCAMPHORStrides Consumer LLCcb5ca02b-0bc1-4b0b-b4b1-abef3222aa562025-04-09WarningsExact identifier
ndc (package): 72927-976-02
ndc (product): 72927-976
ndc11 (package): 72927097602
spl id: b73f0031-d9c9-42f4-b5e8-645dda4d43ac
spl set id: cb5ca02b-0bc1-4b0b-b4b1-abef3222aa56

Reported adverse events (FAERS/openFDA)#

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