Biofreeze

Product NDC: 59316-101
11-digit product format: 593160101
Labeler code: 59316
Product ID: 59316-101_51b434c9-228b-2c05-e063-6394a90a1e94
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: GEL
Route: TOPICAL
Labeler: Reckitt Benckiser LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-08-25
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 35 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	59316-101		D	Discontinued by firm	2026-10-20
excluded package	package	59316-101	59316-101-21	D	Discontinued by firm	2026-10-20
excluded package	package	59316-101	59316-101-25	D	Discontinued by firm	2026-10-20
excluded package	package	59316-101	59316-101-00	D	Discontinued by firm	2026-10-20

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 · 48 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59316-101-25	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59316-101-21	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59316-101-00	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	59316-101-25	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	59316-101-21	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	59316-101-00	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	59316-101-25	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	59316-101-21	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	59316-101-00	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	59316-101-25	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	59316-101-21	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	59316-101-00	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	59316-101-25	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	59316-101-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	59316-101-00	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	59316-101-25	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	59316-101-21	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	59316-101-00	`cdf11ea48f46…`	`ba0047e9e063…`
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	59316-101-25	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	59316-101-21	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	59316-101-00	`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	59316-101-25	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	59316-101-21	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	59316-101-00	`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	59316-101-25	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59316-101-21	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59316-101-00	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	59316-101-25	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	59316-101-21	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	59316-101-00	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	59316-101-25	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	59316-101-21	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	59316-101-00	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	59316-101-25	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	59316-101-21	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	59316-101-00	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: Biofreeze
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	35 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
808955	Internal RxNorm lookup
1043451	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
684faf63-5e44-4471-8384-e8fa7c0d842a	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
59316-101-10	Biofreeze	5 mL in 1 PACKET	GEL	5	43
59316-101-11	Biofreeze	30 mL in 1 BOTTLE	GEL	30	43
59316-101-12	Biofreeze	59 mL in 1 TUBE	GEL	59	43
59316-101-13	Biofreeze	59 mL in 1 BOTTLE, WITH APPLICATOR	GEL	59	43
59316-101-15	Biofreeze	89 mL in 1 BOTTLE, WITH APPLICATOR	GEL	89	43
59316-101-19	Biofreeze	3 mL in 1 PACKET	GEL	3	43
59316-101-20	Biofreeze	118 mL in 1 TUBE	GEL	118	43
59316-101-21	Biofreeze	81 mL in 1 TUBE	GEL	81	43
59316-101-25	Biofreeze	118 mL in 1 TUBE, WITH APPLICATOR	GEL	118	43
59316-101-30	Biofreeze	473 mL in 1 BOTTLE, PUMP	GEL	473	43
59316-101-40	Biofreeze	946 mL in 1 BOTTLE, PUMP	GEL	946	43
59316-101-50	Biofreeze	3785 mL in 1 BOTTLE, PUMP	GEL	3785	43

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Menthol	ACTIVE INGREDIENT	L7T10EIP3A	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
Menthol	ACTIVE MOIETY	L7T10EIP3A	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
CAMPHOR (NATURAL)	INACTIVE INGREDIENT	N20HL7Q941	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
FD&C YELLOW NO. 5	INACTIVE INGREDIENT	I753WB2F1M	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
TROLAMINE	INACTIVE INGREDIENT	9O3K93S3TK	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32
WATER	INACTIVE INGREDIENT	059QF0KO0R	BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH LLC.]	32

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59316-101	BIOFREEZE (MENTHOL) GEL [RB HEALTH (US) LLC]	42	Current NDC, Legacy NDC, 12 package rows	20241228_684faf63-5e44-4471-8384-e8fa7c0d842a.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 122 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sanar Naturals Arnica Reforzada	CAMPHOR	Sanvall Enterprises, Inc	1921a4b1-cd36-195e-e063-6294a90a8793	2024-10-31	Warnings	Exact identifier application number: M017
Sanar Naturals Arnica Pain Releiving Roll On with Camphor	CAMPHOR	Sanvall Enterprises, Inc	173db0e2-611f-55b9-e063-6394a90ac987	2024-10-31	Warnings	Exact identifier application number: M017
Sanar Naturals Camphor	CAMPHOR	Sanvall Enterprises, Inc	1921e851-cf83-0bdb-e063-6294a90a357f	2024-10-31	Warnings	Exact identifier application number: M017
cortisone	HYDROCORTISONE	CVS Pharmacy	c766deac-d993-4e48-a5c3-4cfde7338dff	2024-10-31	Warnings	Exact identifier application number: M017
Walgreens Pain Relieving with Lavender Analgesic	LIDOCAINE HYDROCHLORIDE	Walgreen Company	6c7b39c8-5b65-430a-a529-5b6b14adce18	2024-10-31	Warnings	Exact identifier application number: M017
Walgreens Pain Relieving Plus Turmeric Analgesic	TROLAMINE SALICYLATE	Walgreen Company	f3a121bc-7572-49a4-9822-2b6d858c19d2	2024-10-31	Warnings	Exact identifier application number: M017
dg health hydrocortisone	HYDROCORTISONE	Dolgencorp, LLC	27dc9e09-fc4f-4b66-a303-177725f3a513	2024-10-31	Warnings	Exact identifier application number: M017
basic care hydrocortisone	HYDROCORTISONE	Amazon.com Services LLC	f5419859-3f9f-43ff-9a3f-6aa81af044f0	2024-10-31	Warnings	Exact identifier application number: M017
ARCTIC RELIEF	MENTHOL, UNSPECIFIED FORM	STRATUS PHARMACEUTICALS INC	d27fbc17-46b7-4d52-ba29-c99b6c63144a	2024-10-31	Warnings	Exact identifier application number: M017
Pain Relief Gel-Patch	LIDOCAINE, MENTHOL	R & Y Group, LLC	fe0478d8-2f06-cd56-e053-6294a90a58e5	2024-10-30	Warnings	Exact identifier application number: M017
JOINT-RITIS PAIN RELIEVING ROLL-ON	MENTHOL	Lifeline Naturals of America, Inc.	ec5d99c4-6bba-45d1-84e0-12fb7cb31495	2024-10-30	Warnings	Exact identifier application number: M017
Walgreens Pain Relieving with Turmeric Analgesic	LIDOCAINE HYDROCHLORIDE	Walgreen Company	317ec4fb-cff0-461d-9ca0-299527a3686d	2024-10-30	Warnings	Exact identifier application number: M017
Walgreens Pain Relieving Analgesic	CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE	Walgreen Company	3215a676-104c-43c3-aa36-b30d5b67799a	2024-10-30	Warnings	Exact identifier application number: M017
Ultra-Strength Pain Relief Analgesic	CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM	TARGET CORPORATION	159c5a84-bf68-41dd-a2d3-bc2402037244	2024-10-30	Warnings	Exact identifier application number: M017
DG Health Cold n Hot Pain Relieving Topical Analgesic	MENTHOL, UNSPECIFIED FORM	Dolgencorp Inc	8fe13b85-ab74-42f8-a664-d3d2959921ac	2024-10-30	Warnings	Exact identifier application number: M017
DEBACHERE Butt Balm After Care Antiseptic Pain Relief	BENZOCAINE, BENZALKONIUM CHLORIDE	DE.BACHERE USA LLC	8ba42864-69bf-455c-98d4-7f4ff94edceb	2024-10-29	Warnings	Exact identifier application number: M017
Signature Care Hydrocortisone	HYDROCORTISONE	Safeway	beefab66-b056-4bf1-b047-0780704ab87e	2024-10-29	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	H E B	15eb4676-5f6e-4c28-b5b9-4e45412dc37a	2024-10-29	Warnings	Exact identifier application number: M017
Rael PAIN RELIEF ROLL-ON Analgesic	CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM	Rael, Inc.	e6c49606-7c13-4dc6-a22d-ba54173ba788	2024-10-28	Warnings	Exact identifier application number: M017
Monistat Care Instant Itch Relief	BENZOCAINE	Insight Pharmaceuticals LLC	4e9dc791-419f-4c79-aed4-760f8c17a5dd	2024-10-25	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1043451	BIOFREEZE 3.5 % Topical Gel	PSN	684faf63-5e44-4471-8384-e8fa7c0d842a	43
808955	menthol 3.5 % Topical Gel	PSN	684faf63-5e44-4471-8384-e8fa7c0d842a	43
1043451	menthol 0.035 MG/MG Topical Gel [Biofreeze]	SBD	684faf63-5e44-4471-8384-e8fa7c0d842a	43
808955	menthol 0.035 MG/MG Topical Gel	SCD	684faf63-5e44-4471-8384-e8fa7c0d842a	43
1043451	Biofreeze 0.035 MG/MG Topical Gel	SY	684faf63-5e44-4471-8384-e8fa7c0d842a	43
1043451	Biofreeze 3.5 % Topical Gel	SY	684faf63-5e44-4471-8384-e8fa7c0d842a	43
808955	menthol 3.5 % Topical Gel	SY	684faf63-5e44-4471-8384-e8fa7c0d842a	43

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59316-101-10	59316010110	5 mL in 1 PACKET (59316-101-10)	5 ml	2016-08-25	0000-00-00	No	No	Current
59316-101-11	59316010111	30 mL in 1 BOTTLE (59316-101-11)	30 ml	2016-08-25	0000-00-00	No	No	Current
59316-101-12	59316010112	59 mL in 1 TUBE (59316-101-12)	59 ml	2016-08-25	0000-00-00	No	No	Current
59316-101-13	59316010113	59 mL in 1 BOTTLE, WITH APPLICATOR (59316-101-13)	59 ml	2016-08-25	0000-00-00	No	No	Current
59316-101-15	59316010115	89 mL in 1 BOTTLE, WITH APPLICATOR (59316-101-15)	89 ml	2016-08-25	0000-00-00	No	No	Current
59316-101-19	59316010119	3 mL in 1 PACKET (59316-101-19)	3 ml	2022-01-01	0000-00-00	No	No	Current
59316-101-20	59316010120	118 mL in 1 TUBE (59316-101-20)	118 ml	2016-08-25	0000-00-00	No	No	Current
59316-101-21	59316010121	81 mL in 1 TUBE	81 ml					Historical
59316-101-25	59316010125	118 mL in 1 TUBE, WITH APPLICATOR (59316-101-25)	118 ml	2016-08-25	2021-12-31	No	No	Current
59316-101-30	59316010130	473 mL in 1 BOTTLE, PUMP (59316-101-30)	473 ml	2016-08-25	0000-00-00	No	No	Current
59316-101-40	59316010140	946 mL in 1 BOTTLE, PUMP (59316-101-40)	946 ml	2016-08-25	0000-00-00	No	No	Current
59316-101-50	59316010150	3785 mL in 1 BOTTLE, PUMP (59316-101-50)	3785 ml	2016-08-25	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Biofreeze Pain Relieving Gel	Reckitt Benckiser LLC \| Span Packaging Services dba Multi-Pack Solutions	2026-05-13	HUMAN OTC DRUG LABEL	43