Label: JOINTFLEX- camphor cream
- NDC Code(s): 72927-976-02
- Packager: Strides Consumer LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 10, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses:
- Warnings:
- Do not use
- Ask a doctor befor use if you have
- When using this product
- Stop use and ask doctor if
- Keep out of reach of children.
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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:
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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).
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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
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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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
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INGREDIENTS AND APPEARANCE
JOINTFLEX
camphor creamProduct 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 Drug M 06/01/2021 Labeler - Strides Consumer LLC (116975770) Establishment Name Address ID/FEI Business Operations Beltapharm SPA 429236789 MANUFACTURE(72927-976) , PACK(72927-976)