Biofreeze Colorless

Product NDC: 59316-103
11-digit product format: 593160103
Labeler code: 59316
Product ID: 59316-103_51b597cc-8068-e160-e063-6394a90ac1be
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: 2012-01-03
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 40 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 package	package	59316-103	59316-103-10	D	Discontinued by firm	2026-10-16
excluded package	package	59316-103	59316-103-11	D	Discontinued by firm	2026-10-16
excluded package	package	59316-103	59316-103-15	D	Discontinued by firm	2026-10-16
excluded package	package	59316-103	59316-103-28	D	Discontinued by firm	2026-10-16

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, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	59316-103-10	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	59316-103-11	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	59316-103-28	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	59316-103-15	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	59316-103-10	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	59316-103-11	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	59316-103-28	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	59316-103-15	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	59316-103-10	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	59316-103-11	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	59316-103-28	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	59316-103-15	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	59316-103-10	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	59316-103-11	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	59316-103-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	59316-103-15	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	59316-103-10	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	59316-103-11	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	59316-103-28	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	59316-103-15	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	59316-103-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	59316-103-11	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	59316-103-28	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	59316-103-15	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	59316-103-10	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	59316-103-11	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	59316-103-28	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	59316-103-15	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	59316-103-10	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	59316-103-11	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	59316-103-28	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	59316-103-15	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	59316-103-10	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	59316-103-11	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	59316-103-28	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	59316-103-15	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	59316-103-11	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	59316-103-10	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	59316-103-28	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	59316-103-15	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	59316-103-11	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	59316-103-10	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	59316-103-28	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	59316-103-15	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	59316-103-11	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	59316-103-10	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	59316-103-28	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	59316-103-15	`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 Colorless
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	40 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
415974	Internal RxNorm lookup
1111683	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
939dbbc3-71ec-4990-840e-7c9b8d430562	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
59316-103-10	Biofreeze Colorless	5 mL in 1 BOTTLE	GEL	5	31
59316-103-11	Biofreeze Colorless	3 mL in 1 BOTTLE	GEL	3	31
59316-103-12	Biofreeze Colorless	89 mL in 1 BOTTLE	GEL	89	31
59316-103-15	Biofreeze Colorless	89 mL in 1 BOTTLE, WITH APPLICATOR	GEL	89	31
59316-103-20	Biofreeze Colorless	118 mL in 1 BOTTLE	GEL	118	31
59316-103-28	Biofreeze Colorless	273 mL in 1 BOTTLE	GEL	273	31
59316-103-40	Biofreeze Colorless	946 mL in 1 BOTTLE	GEL	946	31

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59316-103-12	ML - Milliliter	59316-103	b52397a8-ed9d-4dc6-b82e-39964b2d6c6a	1	2018-05-09
59316-103-20	ML - Milliliter	59316-103	700d69bb-759b-4ca7-941b-78f7b2225940	1	2024-06-10
59316-103-40	ML - Milliliter	59316-103	0770d763-3f20-4da3-91bb-9cc65a6fddcf	1	2024-08-12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
ALPHA-TOCOPHEROL ACETATE	INACTIVE INGREDIENT	9E8X80D2L0	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
ARCTIUM LAPPA ROOT	INACTIVE INGREDIENT	597E9BI3Z3	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
ARNICA MONTANA FLOWER	INACTIVE INGREDIENT	OZ0E5Y15PZ	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
CALENDULA OFFICINALIS FLOWER	INACTIVE INGREDIENT	P0M7O4Y7YD	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
CAMPHOR (SYNTHETIC)	INACTIVE INGREDIENT	5TJD82A1ET	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
FRANKINCENSE	INACTIVE INGREDIENT	R9XLF1R1WM	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
GREEN TEA LEAF	INACTIVE INGREDIENT	W2ZU1RY8B0	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
ILEX PARAGUARIENSIS LEAF	INACTIVE INGREDIENT	1Q953B4O4F	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
ISOPROPYL MYRISTATE	INACTIVE INGREDIENT	0RE8K4LNJS	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
MELISSA OFFICINALIS LEAF	INACTIVE INGREDIENT	50D2ZE9219	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
TROLAMINE	INACTIVE INGREDIENT	9O3K93S3TK	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15
WATER	INACTIVE INGREDIENT	059QF0KO0R	BIOFREEZE COLORLESS (MENTHOL) GEL [PERFORMANCE HEALTH LLC]	15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59316-103	BIOFREEZE COLORLESS (MENTHOL) GEL [RB HEALTH (US) LLC]	30	Current NDC, Legacy NDC, 7 package rows	20241228_939dbbc3-71ec-4990-840e-7c9b8d430562.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 14 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Roll Pain Away	CAPSAICIN	PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA	547e647b-0205-221c-e063-6294a90a757c	2026-06-17	Warnings	Exact identifier application number: M017
Roll Pain Away Lemongrass	CAPSAICIN	PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA	547ef5c0-bc31-d83e-e063-6394a90abfa6	2026-06-17	Warnings	Exact identifier application number: M017
Roll Pain Away Lavender	CAPSAICIN	PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA	547ef2d9-f5c7-9de1-e063-6394a90a218b	2026-06-17	Warnings	Exact identifier application number: M017
Velloryn EXTRA STRENGTH NEUROPATHY	VELLORYN EXTRA STRENGTH NEUROPATHY	GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd	547f755f-c65c-37ef-e063-6394a90aa220	2026-06-17	Warnings	Exact identifier application number: M017
Neoteric Diabetic Skin Care 4 oz.	DIMETHICONE	RNA PHARMA LLC	536f4e79-201b-7100-e063-6394a90a4f82	2026-06-16	Warnings	Exact identifier application number: M017
Medi First Extra Strength Itch Relief	DIPHENHYDRAMINE, ZINC ACETATE	Unifirst First Aid Corporation	54614e5b-8c72-d308-e063-6294a90a405d	2026-06-16	Warnings	Exact identifier application number: M017
Blue Ice Analgesic	MENTHOL	Delon Laboratories (1990) Ltd	184ed488-6e62-40c6-bb71-1d523280fd6b	2026-06-16	Warnings	Exact identifier application number: M017
Medi-First Hydrocortisone 1 % Anti-Itch Cream	HYDROCORTISONE	Unifirst First Aid Corporation	49f04e5d-746d-cbe9-e063-6294a90a7e88	2026-06-16	Warnings	Exact identifier application number: M017
Lidozall Pro	LIDOCAINE HYDROCHLORIDE	V2 Pharma LLC	ecc26ba7-4ff6-43e6-bfb9-91a9cbb509ff	2026-06-16	Warnings	Exact identifier application number: M017
Tiger Balm Pain Relieving Cool	CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM	Haw Par Healthcare Ltd.	41590ba1-32bb-4352-97ba-d6a3cc9d0546	2026-06-15	Warnings	Exact identifier application number: M017
HIGH POTENCY PAIN RELIEF	CAPSAICIN	Xiamen Weisiqi Technology Co., Ltd.	543949a4-86ed-3734-e063-6394a90a24f2	2026-06-14	Warnings	Exact identifier application number: M017
Natucure HEMORRHOID	LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID	Jiangxi Yudexi Pharmaceutical Co., LTD	49e402ed-d314-e896-e063-6294a90a826b	2026-06-14	Warnings	Exact identifier application number: M017
Nieapf NUMBING	LIDOCAINE 4% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	49e7534f-bccf-4ef4-e063-6294a90aeb7f	2026-06-14	Warnings	Exact identifier application number: M017
HEALMUSZ NUMBING	HEALMUSZ NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	49976ff7-49a4-e4ed-e063-6294a90a3f78	2026-06-14	Warnings	Exact identifier application number: M017
HEALMUSZ HEMORRHOID FISSURE	LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID FISSURE	Jiangxi Yudexi Pharmaceutical Co., LTD	4a342ac0-6a8d-3408-e063-6394a90a9a10	2026-06-14	Warnings	Exact identifier application number: M017
BOTASUN QUIT SMOKING Nicotine	NICOTINE18% MENTHOL 0.3% QUIT SMOKING NICOTINE	Jiangxi Yudexi Pharmaceutical Co., LTD	4fa00db9-def5-dcfa-e063-6394a90ac8c2	2026-06-14	Warnings	Exact identifier application number: M017
HEALMUSZ NUMBING	MENTHOL 5% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	4cbb7df5-5771-ce4b-e063-6294a90aab80	2026-06-14	Warnings	Exact identifier application number: M017
HEALMUSZ ECZEMA	HYDROCORTISONE 1% ECZEMA	Jiangxi Yudexi Pharmaceutical Co., LTD	511e54e0-2abe-fb76-e063-6294a90ada68	2026-06-14	Warnings	Exact identifier application number: M017
Hydrocortisone 1% Anti-ItchCream	HYDROCORTISONE	Acme United Corporation	5425fc2b-4f25-3e64-e063-6394a90aff49	2026-06-13	Warnings	Exact identifier application number: M017
Icy Hot Pain Relieving Balm	MENTHOL AND METHYL SALICYLATE	Chattem, Inc.	40c8c02f-fa5f-4e80-81a0-48271fa6f94b	2026-06-12	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
1111683	BIOFREEZE 4 % Topical Gel	PSN	939dbbc3-71ec-4990-840e-7c9b8d430562	31
415974	menthol 4 % Topical Gel	PSN	939dbbc3-71ec-4990-840e-7c9b8d430562	31
1111683	menthol 0.04 MG/MG Topical Gel [Biofreeze]	SBD	939dbbc3-71ec-4990-840e-7c9b8d430562	31
415974	menthol 0.04 MG/MG Topical Gel	SCD	939dbbc3-71ec-4990-840e-7c9b8d430562	31
1111683	Biofreeze 0.04 MG/MG Topical Gel	SY	939dbbc3-71ec-4990-840e-7c9b8d430562	31
1111683	Biofreeze 4 % Topical Gel	SY	939dbbc3-71ec-4990-840e-7c9b8d430562	31
415974	menthol 4 % Topical Gel	SY	939dbbc3-71ec-4990-840e-7c9b8d430562	31
1111683	BIOFREEZE 4 % Topical Gel	PSN	cc1cba14-da40-4d7d-b522-b5c648798e96	4
415974	menthol 4 % Topical Gel	PSN	cc1cba14-da40-4d7d-b522-b5c648798e96	4
1111683	menthol 0.04 MG/MG Topical Gel [Biofreeze]	SBD	cc1cba14-da40-4d7d-b522-b5c648798e96	4
415974	menthol 0.04 MG/MG Topical Gel	SCD	cc1cba14-da40-4d7d-b522-b5c648798e96	4
1111683	Biofreeze 0.04 MG/MG Topical Gel	SY	cc1cba14-da40-4d7d-b522-b5c648798e96	4
1111683	Biofreeze 4 % Topical Gel	SY	cc1cba14-da40-4d7d-b522-b5c648798e96	4
415974	menthol 4 % Topical Gel	SY	cc1cba14-da40-4d7d-b522-b5c648798e96	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59316-103-10	59316010310	5 mL in 1 BOTTLE	5 ml					Historical
59316-103-11	59316010311	3 mL in 1 BOTTLE (59316-103-11)	3 ml	2012-01-03	2021-12-31	No	No	Current
59316-103-12	59316010312	89 mL in 1 BOTTLE (59316-103-12)	89 ml	2016-09-19	0000-00-00	No	No	Current
59316-103-15	59316010315	89 mL in 1 BOTTLE, WITH APPLICATOR	89 ml					Historical
59316-103-20	59316010320	118 mL in 1 BOTTLE (59316-103-20)	118 ml	2012-01-03	0000-00-00	No	No	Current
59316-103-28	59316010328	273 mL in 1 BOTTLE	273 ml					Historical
59316-103-40	59316010340	946 mL in 1 BOTTLE (59316-103-40)	946 ml	2012-01-03	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Biofreeze ® Colorless	Reckitt Benckiser LLC	2026-05-13	HUMAN OTC DRUG LABEL	31
Biofreeze ® Colorless	A-S Medication Solutions	2024-11-11	HUMAN OTC DRUG LABEL	4
Biofreeze Colorless Gel	Performance Health LLC	2019-06-18	HUMAN OTC DRUG LABEL	3