Jointflex

Product NDC: 72927-904
11-digit product format: 729270904
Labeler code: 72927
Product ID: 72927-904_064c9f01-0578-4506-862f-306442181f53
Type: HUMAN OTC DRUG
Nonproprietary name: Jointflex
Dosage form: CREAM
Route: TOPICAL
Labeler: Strides Consumer LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-08-02
Substance: CAMPHOR (SYNTHETIC)
Active strength: 3.2 g/100g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72927-904-04	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72927-904-03	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72927-904-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72927-904-04	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72927-904-03	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72927-904-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72927-904-04	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72927-904-03	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72927-904-01	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Jointflex
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	3.2 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5TJD82A1ET	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2181415	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
b82ec69c-bd00-400b-bd94-ac15fb620f9b	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
72927-904-01	2025-02-07	JointFlex® Pain Relief Cream Drug Facts
72927-904-03	2025-02-07	JointFlex® Pain Relief Cream Drug Facts
72927-904-04	2025-02-07	JointFlex® Pain Relief Cream Drug Facts
72927-904-01	2025-01-30	JointFlex® Pain Relief Cream Drug Facts
72927-904-03	2025-01-30	JointFlex® Pain Relief Cream Drug Facts
72927-904-04	2025-01-30	JointFlex® Pain Relief Cream Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72927-904-01	Jointflex	114 g in 1 TUBE	CREAM	114	5
72927-904-01	Jointflex	1 in 1 CARTON	CREAM	1	5
72927-904-03	Jointflex	1 in 1 CARTON	CREAM	1	5
72927-904-03	Jointflex	28 g in 1 TUBE	CREAM	28	5
72927-904-04	Jointflex	28 g in 1 TUBE	CREAM	28	5
72927-904-04	Jointflex	1 in 1 CARTON	CREAM	1	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72927-904	JOINTFLEX CREAM [STRIDES CONSUMER LLC]	5	Current NDC, Legacy NDC, 6 package rows	20250410_b82ec69c-bd00-400b-bd94-ac15fb620f9b.zip

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 80 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
HealthWise Overnight Menthol Patch	MENTHOL	Veridian Healthcare	6379f50d-2878-46ca-8acb-71c4554585e9	2025-08-28	Warnings	Exact identifier application number: M017
Anti Itch Maximum Relief	PRAMOXINE HYDROCHLORIDE AND MENTHOL	Natureplex LLC	75de3d5e-ecbe-4d04-a39d-792200e6ee32	2025-08-28	Warnings	Exact identifier application number: M017
NicDuic Quit Smoking Nicotine Patches	NICOTINE TRANSDERMAL PATCHES	Shenzhen Paxi Trading Co., Ltd.	3d5718f3-c175-6b64-e063-6394a90aa6f1	2025-08-27	Warnings	Exact identifier application number: M017
ARCTIC HEAT	MENTHOL, METHYL SALICYLATE	Renu Laboratories, LLC	402df5c1-b8cb-17a2-e054-00144ff8d46c	2025-08-27	Warnings	Exact identifier application number: M017
PROHEAL HYDROCORTISONE 1% MAXIMUM STRENGTH PLUS ALOE	HYDROCORTISONE	Click Industries LLC	328c389c-7e05-4892-a9b3-b6a753f4935a	2025-08-25	Warnings	Exact identifier application number: M017
Yeheal	CAMPHOR, MENTHOL, ISOPROPYL ALCOHOL	Shenzhen Yeheal Biotechnology Co., Ltd	3cf1bc74-3060-6d63-e063-6294a90a9f5c	2025-08-22	Warnings	Exact identifier application number: M017
Dermedial Anti-Ouch	MENTHOL	Natures Formulae Health Products Ltd.	3ce29160-3964-e435-e063-6394a90abb38	2025-08-21	Warnings	Exact identifier application number: M017
SUGARLOAF ORGANICS MENTHOL REVIVE	MENTHOL	RENU LABORATORIES, LLC	fa2f9539-b703-a00b-e053-6394a90ae309	2025-08-21	Warnings	Exact identifier application number: M017
Camphor 4% Plus Menthol 10%	CAMPHOR 4% PLUS MENTHOL 10%	PureTek Corporation	3cab26e4-e377-f26a-e063-6394a90a17af	2025-08-20	Warnings	Exact identifier application number: M017
Capsaicin 0.035% Cream	CAPSAICIN 0.035% CREAM	Puretekcorp	3cbc73b6-8c58-8f23-e063-6394a90a71a3	2025-08-20	Warnings	Exact identifier application number: M017
Game On	MENTHOL, METHYL SALICYLATE	Natural Essentials, Inc.	3cd20f1f-033f-f698-e063-6294a90a89eb	2025-08-20	Warnings	Exact identifier application number: M017
ELAIMEI Numbing Cream	LIDOCAINE 4%	Shenzhen Shandian Jingling Technology Co., Ltd.	37ac13b2-ca55-0e28-e063-6294a90a000e	2025-08-19	Warnings	Exact identifier application number: M017
Calamine Plus Pramoxine HCl	CALAMINE PLUS SPRAY	FSA Store Inc.	3cd18f96-34f7-3f2c-e063-6294a90a3b7e	2025-08-19	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE SPRAY	FSA Store Inc.	3ce24b87-55ac-0bbd-e063-6294a90ab582	2025-08-19	Warnings	Exact identifier application number: M017
Fast Freeze Pain Relieving	MENTHOL, UNSPECIFIED FORM	NATURAL ESSENTIALS, INC.	15a26af1-ca5a-40fc-a411-6c0e8ae18fbb	2025-08-18	Warnings	Exact identifier application number: M017
Orythia Maximum Strength Lidocaine Pain Relieving	LIDOCAINE	Planet (Anhui) Pharmaceutical Co., Ltd.	6d6b59f9-f614-4e3c-b07b-32b4591d39f2	2025-08-18	Warnings	Exact identifier application number: M017
Ocean Potion Suncare Ice Plus Pain Relieving Soothing	LIDOCAINE	GNL BRANDS INTERNATIONAL, LLC	3c69654c-cba6-dfef-e063-6394a90ad479	2025-08-15	Warnings	Exact identifier application number: M017
Earth Mama Medicated Herbal Lip Balm	MENTHOL	Eleeo Brands LLC	3c6c16bb-1f4b-b851-e063-6294a90a7404	2025-08-15	Warnings	Exact identifier application number: M017
Lidocaine Hydrochloride	LIDOCAINE HYDROCHLORIDE	Cintas First Aid & Safety	96f17095-31f3-4b8a-ab22-0caaefaa7476	2025-08-15	Warnings	Exact identifier application number: M017
MedPride Cold Ice Analgesic Gel	MENTHOL	SHIELD LINE LLC	860a2c86-b240-4e0e-e053-2a91aa0a333a	2025-08-15	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2181415	camphor 3.2 % Topical Cream	PSN	b82ec69c-bd00-400b-bd94-ac15fb620f9b	5
2181415	camphor 32 MG/ML Topical Cream	SCD	b82ec69c-bd00-400b-bd94-ac15fb620f9b	5
2181415	camphor 3.2 % Topical Cream	SY	b82ec69c-bd00-400b-bd94-ac15fb620f9b	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72927-904-01	72927090401	1 TUBE in 1 CARTON (72927-904-01) / 114 g in 1 TUBE	1 tube	2019-08-02	0000-00-00	No	No	Current
72927-904-03	72927090403	1 TUBE in 1 CARTON (72927-904-03) / 28 g in 1 TUBE	1 tube	2019-08-02		No	No	Current
72927-904-04	72927090404	1 TUBE in 1 CARTON (72927-904-04) / 28 g in 1 TUBE	1 tube	2019-08-02		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
JointFlex® Pain Relief Cream Drug Facts	Strides Consumer LLC \| Beltapharm SPA	2025-04-09	HUMAN OTC DRUG LABEL	5