Jointflex

Camphor


Strides Consumer Llc
Human Otc Drug
NDC 72927-944
Jointflex also known as Camphor is a human otc drug labeled by 'Strides Consumer Llc'. National Drug Code (NDC) number for Jointflex is 72927-944. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Jointflex drug includes Camphor (synthetic) - 3.2 g/100g . The currest status of Jointflex drug is Active.

Drug Information:

Drug NDC: 72927-944
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Jointflex
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Camphor
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Strides Consumer Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Cream
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:CAMPHOR (SYNTHETIC) - 3.2 g/100g
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:TOPICAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: OTC MONOGRAPH NOT FINAL
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 09 Mar, 2020
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 17 Dec, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: part348
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Strides Consumer LLC
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:2181415
2282659
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0372917000245
UPC stands for Universal Product Code.
UNII:5TJD82A1ET
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
72927-944-011 TUBE in 1 CARTON (72927-944-01) / 85 g in 1 TUBE09 Mar, 2020N/ANo
72927-944-021 TUBE in 1 CARTON (72927-944-02) / 28 g in 1 TUBE01 Sep, 2021N/ANo
72927-944-031 TUBE in 1 CARTON (72927-944-03) / 28 g in 1 TUBE26 Mar, 2021N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Purpose:

Purpose topical analgesic

Product Elements:

Jointflex camphor camphor (synthetic) camphor (synthetic) acetylated lanolin alkyl (c12-15) benzoate aloe vera leaf alpha-tocopherol acetate carbomer 1342 carbomer interpolymer type a (55000 cps) chondroitin sulfate (shark) diazolidinyl urea dimethicone edetate disodium glucosamine sulfate potassium chloride glycerin glyceryl monostearate hydroxylated lanolin hypromelloses iodopropynyl butylcarbamate methyl gluceth-20 methyl glucose sesquistearate panthenol peppermint oil polyoxyl 40 stearate polysorbate 20 potassium hydroxide shark cartilage turmeric oil water

Indications and Usage:

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

Warnings:

Warnings: for external use only.

Do Not Use:

Warnings: for external use only.

When Using:

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

Dosage and Administration:

Directions: 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 ® pain relieving cream 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

Stop Use:

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

Package Label Principal Display Panel:

Package label.principal display panel 8 week challenge for pain relief* #1 clinically recommended† joint pain cream jointflex ® - pain relief cream with natural turmeric effectively reduces joint pain immediate & long lasting relief* contains glucosamine & chondroitin** no stain/ no grease/ pleasant scent net wt 3 oz (85g) deep penetrating fusome ® technology quick & effective penetration targeted pain relief long lasting relief when used daily flex your freedom ™ relieves back, neck, shoulder, knees, elbow, foot, ankle, leg hand and wrist pain ndc 72927-944-01 visit www.jointflex.com for more information * when applied as directed ** for skin conditioning 011-1630c-r02 8 week challenge for pain relief* 100% money back guarantee* effectively reduces joint pain jointflex ® - pain relief cream with natural turmeric immediate & long lasting relief* contains glucosamine & chondroitin** no stain/ no grease/ pleasant scent deep penetrating fusome ® technology quick & effective penetration targeted pain relief long lasting relief when used daily flex your freedom ™ relieves back, neck, shoulder, knees, elbow, foot, ankle, leg hand and wrist pain net wt 1 oz (28g) jointflex ® guarantee "if you use jointflex as directed and are not completely amazed with the pain relief you received, simply return the tube (even if it's empty) and the cash register receipt to the address below for a full refund. no questions asked." questions or comments? call (866)-235-4581. strides consumer llc, east brunswick, nj 08816 ndc 72927-944-03 visit www.jointflex.com for more information licensed user of trademarks. © 2020 strides consumer llc sample not for retail sale. * when applied as directed ** for skin conditioning 8 week challenge for pain relief* 100% money back guarantee* effectively reduces joint pain jointflex ® - pain relief cream with natural turmeric immediate & long lasting relief* contains glucosamine & chondroitin** no stain/ no grease/ pleasant scent deep penetrating fusome ® technology quick & effective penetration targeted pain relief long lasting relief when used daily flex your freedom ™ relieves back, neck, shoulder, knees, elbow, foot, ankle, leg hand and wrist pain net wt 1 oz (28g) jointflex ® guarantee "if you use jointflex as directed and are not completely amazed with the pain relief you received, simply return the tube (even if it's empty) and the cash register receipt to the address below for a full refund. no questions asked." questions or comments? call (866)-235-4581. strides consumer llc, east brunswick, nj 08816 ndc 72927-944-02 visit www.jointflex.com for more information licensed user of trademarks. © 2020 strides consumer llc * when applied as directed ** for skin conditioning jointflex turmeric - 3 oz 28g carton image carton-1oz-for sale

Further Questions:

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. © 2020 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


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.