Blue Ice Analgesic

Product NDC: 61734-021
11-digit product format: 617340021
Labeler code: 61734
Product ID: 61734-021_546439e4-4be6-7792-e063-6394a90a18f9
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: GEL
Route: TOPICAL
Labeler: Delon Laboratories (1990) Ltd
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2010-05-07
Substance: MENTHOL
Active strength: 2 g/100g
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	61734-021	61734-021-01	D	Discontinued by firm		2026-10-15
excluded package	package	61734-021	61734-021-02	D	Discontinued by firm		2026-10-15

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 · 24 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	61734-021-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	61734-021-02	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	61734-021-01	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	61734-021-02	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	61734-021-01	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	61734-021-02	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	61734-021-01	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	61734-021-02	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	61734-021-01	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	61734-021-02	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	61734-021-02	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	61734-021-01	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	61734-021-02	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	61734-021-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	61734-021-02	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	61734-021-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	61734-021-02	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	61734-021-01	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	61734-021-02	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	61734-021-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	61734-021-02	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	61734-021-01	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	61734-021-02	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	61734-021-01	`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: Blue Ice Analgesic
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	2 g/100g

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 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
311502	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
184ed488-6e62-40c6-bb71-1d523280fd6b	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6e3c022f-0786-43f1-8857-edff89d5153f	Product name	1	20260309
efd58652-cb8f-4018-91ca-4b0eb2ff729f	Product name	7	20240226
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829
2641ccb3-721d-4fbf-9f2f-ca2f18157a62	Product name	3	20210309
e7e58cd3-cacb-49df-8d34-1ee335614abb	Product name	1	20150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
61734-021-01	Blue Ice Analgesic	100 g in 1 BOTTLE, PUMP	GEL	100	19
61734-021-02	Blue Ice Analgesic	113.56 g in 1 CONTAINER	GEL	113.56	19
61734-021-03	Blue Ice Analgesic	227 g in 1 CONTAINER	GEL	227	19

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
Menthol	ACTIVE INGREDIENT	L7T10EIP3A	BLUE ICE ANALGESIC (MENTHOL) GEL [DELON LABORATORIES (1990) LTD]	5
Menthol	ACTIVE MOIETY	L7T10EIP3A	BLUE ICE ANALGESIC (MENTHOL) GEL [DELON LABORATORIES (1990) LTD]	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61734-021	BLUE ICE ANALGESIC (MENTHOL) GEL [DELON LABORATORIES (1990) LTD]	18	Current NDC, Legacy NDC, 3 package rows	20250313_184ed488-6e62-40c6-bb71-1d523280fd6b.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 111 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Medicated Pain Relief Patches	CAMPHOR, MENTHOL, METHYL SALICYLATE	Meijer Distribution Inc	75c6fcd5-185c-4203-b604-19ce801c865f	2024-12-18	Warnings	Exact identifier application number: M017
MEIJER PAIN RELIEF PATCHES	LIDOCAINE	Meijer Distribution Inc	aa5da66d-3ba9-4120-be35-44bec475761a	2024-12-18	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief Roll-On	LIDOCAINE 4%	CVS Pharmacy	8a9757e3-0bfc-a1e2-e053-2a95a90a6da3	2024-12-18	Warnings	Exact identifier application number: M017
Dollar General Cold-Hot Medicated Patches	MENTHOL	DOLGENCORP, LLC	c6e0388b-af9e-4e51-8f94-6788185c31a0	2024-12-18	Warnings	Exact identifier application number: M017
THERA CARE PAIN THERAPY	LIDOCAINE	Veridian Healthcare	e023bb5a-a4bc-4681-a1f4-48ca0d2cb102	2024-12-18	Warnings	Exact identifier application number: M017
TheraCare Medicated Pain Relief Patches	CAMPHOR, MENTHOL, METHYL SALICYLATE	Veridian Healthcare	f6f3c9c0-d6e3-75a3-e053-6294a90a1965	2024-12-18	Warnings	Exact identifier application number: M017
Good Sense Hot and Cold Medicated Patch	MENTHOL	GOOD SENSE	1b16c3e5-a29f-4043-94e6-0a0e0ea3d93e	2024-12-18	Warnings	Exact identifier application number: M017
Hunter Beach 4%	LIDOCAINE	HUNTERS BEACH LIFE	f2ef9c12-6e42-486b-b6f2-0ad534e94294	2024-12-18	Warnings	Exact identifier application number: M017
Hunter Beach 4%	LIDOCAINE	HUNTERS BEACH LIFE	05a9605b-0d01-4333-8e54-7202e7c31c49	2024-12-18	Warnings	Exact identifier application number: M017
Ultra Strength Muscle Rub	CAMPHOR, MENTHOL, METHYL SALICYLATE	The Mentholatum Company	32b64985-0e2f-49ee-9840-946d7279fee7	2024-12-17	Warnings	Exact identifier application number: M017
WellPatch Warming Pain Relief	CAPSAICIN	The Mentholatum Company	ec583129-55fc-4ab1-94e5-9c900b5d95ef	2024-12-17	Warnings	Exact identifier application number: M017
CVS Health Cold and Hot Pain Relieving Extra Strength	MENTHOL, METHYL SALICYLATE	CVS Pharmacy	1ca1a631-cb2c-46cd-bd41-05469b08d208	2024-12-17	Warnings	Exact identifier application number: M017
Mentholatum Pain Relieving	MENTHOL, METHYL SALICYLATE	The Mentholatum Company	0056b952-9870-485a-9f35-f985472875a9	2024-12-17	Warnings	Exact identifier application number: M017
Mentholatum Lidocaine Heat	LIDOCAINE HCL	The Mentholatum Company	cc2ef25a-b569-4d48-a666-899f710b4b34	2024-12-17	Warnings	Exact identifier application number: M017
Rite Aid Muscle Rub Ultra Strength	CAMPHOR, MENTHOL, METHYL SALICYLATE	Rite Aid Corporation	039fff40-b5ba-42cb-932c-8a70ca92759d	2024-12-17	Warnings	Exact identifier application number: M017
Signature Care Cold and Hot Medicated	MENTHOL	Safeway	88f59f95-0a7c-458c-949c-0dff16ad94e4	2024-12-17	Warnings	Exact identifier application number: M017
Equate Cool and Heat	MENTHOL, METHYL SALICYLATE	Wal-Mart Stores Inc	c5ab2426-eeca-4ba4-9f00-7790d2176471	2024-12-17	Warnings	Exact identifier application number: M017
Equate Capsaicin Pain Relieving	CAPSAICIN	Wal-Mart Stores Inc	745b2cf5-2599-4383-818b-19fed248a11f	2024-12-17	Warnings	Exact identifier application number: M017
CVS Health Muscle Rub Ultra Strength	CAMPHOR, MENTHOL, METHYL SALICYLATE	CVS Pharmacy	4fc0d6bb-efa7-40cf-a6d5-e0feaa93c80a	2024-12-17	Warnings	Exact identifier application number: M017
DG Health Maximum Strength Pain Relieving Cleansing	BENZALKONIUM CL, LIDOCAINE HCL	Dollar General Corporation	64f69315-77a3-49dc-940d-efd7a29c6645	2024-12-17	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
311502	menthol 2 % Topical Gel	PSN	184ed488-6e62-40c6-bb71-1d523280fd6b	19
311502	menthol 0.02 MG/MG Topical Gel	SCD	184ed488-6e62-40c6-bb71-1d523280fd6b	19
311502	menthol 2 % Topical Gel	SY	184ed488-6e62-40c6-bb71-1d523280fd6b	19
311502	menthol 2 % topical stick	SY	184ed488-6e62-40c6-bb71-1d523280fd6b	19

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
61734-021-01	61734002101	100 g in 1 BOTTLE, PUMP	100 g					Historical
61734-021-02	61734002102	113.56 g in 1 CONTAINER	113.56 g					Historical
61734-021-03	61734002103	227 g in 1 CONTAINER (61734-021-03)	227 g	2010-05-07	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Blue Ice Gel	Delon Laboratories (1990) Ltd \| Laboratoires Delon	2026-06-16	HUMAN OTC DRUG LABEL	20