Biofreeze

Product NDC: 59316-101
Requested package NDC: 59316-101-12
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

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 1 of 157 · 3,129 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
JenGufun LIDOCAINE KNEE Patch	LIDOCAINE KNEE PATCH	Henan Kangdi Medical Devices Co., Ltd.	5b1d8508-b993-7a8d-e063-6294a90ae306	2026-09-10	Warnings	Exact identifier application number: M017
Wart Corn Remover	SALICYLIC ACID	HONG KONG FOREVER YOUNG TRADING CO., LIMITED	5b0cd6e0-f220-4ebd-e063-6294a90ade67	2026-09-09	Warnings	Exact identifier application number: M017
Magic Cream	PAIN RELIEVING OINTMENT	Jiangxi Baikang Medical Products Co., Ltd.	5b0f2515-47e9-603f-e063-6294a90af9d4	2026-09-09	Warnings	Exact identifier application number: M017
Burn Gel	LIDOCAINE HCI	Trifecta Pharmaceuticals USA LLC	e9d3e9be-1036-fad0-e053-2a95a90a6efe	2026-09-09	Warnings	Exact identifier application number: M017
4% Lidocaine Pain Relief Patch	LIDOCAINE 4%	Guangxi Keyun E-commerce Co., Ltd.	5b197cd8-542f-38b4-e063-6294a90ad7d3	2026-09-09	Warnings	Exact identifier application number: M017
Pain Relieving Lidocaine Patch	LIDOCAINE	YYBA CORP	af8c84fd-224c-72b3-e053-2a95a90a9568	2026-09-07	Warnings	Exact identifier application number: M017
American Safety First Aid	LIDOCAINE HCL	Orazen Inc	ea2f776b-dfd0-6ce4-e053-2995a90af009	2026-09-07	Warnings	Exact identifier application number: M017
MEDI-FIRST Topical Analgesic	LIDOCAINE HCI	Ultra Distributors Inc	b6f288f7-9ae3-215e-e053-2a95a90aedf6	2026-09-07	Warnings	Exact identifier application number: M017
MEDI-FIRST	BENZALKONIUM CHLORIDE, LIDOCAINE	Orazen Inc	f508434f-5948-7134-e053-2a95a90a03d7	2026-09-05	Warnings	Exact identifier application number: M017
MEDI-FIRST	BENZALKONIUM CHLORIDE, LIDOCAINE	Orazen Inc	f522fb0b-3d86-b228-e053-2a95a90a55e9	2026-09-05	Warnings	Exact identifier application number: M017
SurviveX Anti-itch Cream	SURVIVEX HYDROCORTISONE	Nantong Health & Beyond Hygienic Products Inc.	5a7a1141-d3b1-0ee8-e063-6294a90a16aa	2026-09-04	Warnings	Exact identifier application number: M017
NeuroNesic Pain Relieving Cream	CAPSAICIN	Blaine Labs Inc.	7107c13d-bf59-4c0a-84fe-725a9fca2691	2026-09-04	Warnings	Exact identifier application number: M017
FREEZE EASE	MENTHOL 4%	Global America Group LLC	16553eda-ec34-485a-a11c-f51260efd9fa	2026-09-03	Warnings	Exact identifier application number: M017
Neoteric Diabetic Skin Care 1 oz.	DIMETHICONE	RNA PHARMA LLC	5a944486-9591-f583-e063-6394a90aa04b	2026-09-03	Warnings	Exact identifier application number: M017
Equate Menthol Pain Relieving	MENTHOL	Wal-Mart Stores Inc	d5b0a7f1-4e23-426b-bb7e-aaa251ad4ffc	2026-09-03	Warnings	Exact identifier application number: M017
ZHI Technologies	LIDOCAINE, MENTHOL	ZHI Technologies, Inc.	6717e995-4d2d-49e8-8ecf-7c62557dfdef	2026-09-03	Warnings	Exact identifier application number: M017
Komxsum LIDOCAINE Cream	LIDOCAINE 4% CREAM	Wenzhou Yuyuan Pharmaceutical Co., Ltd.	5a9feae0-9be4-e736-e063-6294a90abe55	2026-09-03	Warnings	Exact identifier application number: M017
FREEZE EASE Roll-On	MENTHOL	Global America Group LLC	1869cc0d-a056-45de-aede-23b09b61ed12	2026-09-02	Warnings	Exact identifier application number: M017
Gaimoa Lidocaine Pain Relief Gel Patches	LIDOCAINE PAIN RELIEF GEL PATCHES	Henan Enokon Medical Instrument Co., Ltd.	5a68fe67-5c15-af9a-e063-6294a90a7ec1	2026-09-01	Warnings	Exact identifier application number: M017
CVS Cortisone Liquid	HYDROCORTISONE	CVS Pharmacy	42df45a9-d449-090a-e063-6394a90a9ee4	2026-09-01	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
59316-101-12	59316010112	59 mL in 1 TUBE (59316-101-12)	59 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