JOINTFLEX- camphor cream

Jointflex by

Drug Labeling and Warnings

Jointflex by is a Otc medication manufactured, distributed, or labeled by Strides Consumer LLC, Beltapharm SPA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Camphor (3.2%)

Purpose

Topical analgesic

Uses:

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

• simple backache
• arthritis
• strains
• bruises
• sprains

Warnings:

For external use only.

Do not use

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

Ask a doctor befor use if you have

• redness over the affected area

When using this product

• 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

• 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.

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

Directions:

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:

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

Inactive ingredients:

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?

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

INGREDIENTS AND APPEARANCE

JOINTFLEX 
camphor cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72927-976
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	3.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ACETYLATED LANOLIN (UNII: 2X654GD19H)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER 1342 (UNII: 809Y72KV36)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
DIMETHICONE (UNII: 92RU3N3Y1O)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLUCOSAMINE SULFATE POTASSIUM CHLORIDE (UNII: 15VQ11I66N)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
HYDROXYLATED LANOLIN (UNII: EOI0B9800C)
HYPROMELLOSES (UNII: 3NXW29V3WO)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)
PANTHENOL (UNII: WV9CM0O67Z)
PEPPERMINT OIL (UNII: AV092KU4JH)
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SHARK CARTILAGE (UNII: D2YCN1I522)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72927-976-02	1 in 1 CARTON	06/01/2021
1		99 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/01/2021

Labeler - Strides Consumer LLC (116975770)

Establishment
Name	Address	ID/FEI	Business Operations
Beltapharm SPA		429236789	MANUFACTURE(72927-976) , PACK(72927-976)