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 101 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Menthol Pain Relief Gel-Roll On	MENTHOL	Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.	0bd62de8-ce8b-c110-e063-6294a90a98cb	2025-02-07	Warnings	Exact identifier application number: M017
Menthol Pain Relief Gel-Tube	MENTHOL	Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.	0bb07892-824e-8691-e063-6294a90a3891	2025-02-07	Warnings	Exact identifier application number: M017
Olu Pain Management	LIDOCAINE AND CAMPHOR	Olakino Therapeutics LLC	2a41a621-c6f7-5819-e063-6394a90ae67d	2025-02-07	Warnings	Exact identifier application number: M017
Pain Reliveing Patch	LIDOCAINE 4%	simple diagnostics	02ed0b27-bba9-ec0c-e063-6294a90a014d	2025-02-07	Warnings	Exact identifier application number: M017
FlexDermal Pain Relieving Roll-On	MENTHOL	SOLVADERM LLC	d4d8050e-0761-4491-8635-39c806701eb5	2025-02-06	Warnings	Exact identifier application number: M017
Lipo Flavonoid Ear Pain Relief Drops with 4% Lidocaine	LIPO FLAVONOID EAR PAIN RELIEF DROPS WITH 4% LIDOCAINE	Clarion Brands LLC	2d7e9f6a-0f21-b103-e063-6294a90a912f	2025-02-06	Warnings	Exact identifier application number: M017
signature care Hydrocortisone	HYDROCORTISONE	Safeway	9fe16fc5-77e3-47f5-a943-85bc6565c0d4	2025-02-06	Warnings	Exact identifier application number: M017
Methyl Salicylate	METHYL SALICYLATE	PHARMACURE LLC	8803ae01-ea48-46c2-ab64-bb273de605ac	2025-02-05	Warnings	Exact identifier application number: M017
Hempvana Maximum Strength Pain Relief Cream 10% Trolamine Salicylate	TROLAMINE SALICYLATE	TELEBRANDS CORP	2d685602-5cd6-3b36-e063-6394a90a3c5d	2025-02-05	Warnings	Exact identifier application number: M017
Lidocore	LIDOCAINE	iON Pharma, LLC	204c3e50-1ac8-f442-e063-6294a90ae7b5	2025-02-05	Warnings	Exact identifier application number: M017
Methyl Salicylate	METHYL SALICYLATE	PHARMACURE LLC	2c32cfed-2022-4e7c-ae9c-ba22dbb560af	2025-02-04	Warnings	Exact identifier application number: M017
Capsaicin	CAPSAICIN	PHARMACURE LLC	b2b2de93-d957-43d7-a2a8-b46bcaea1f0d	2025-02-04	Warnings	Exact identifier application number: M017
Hempvana Maximum Strength Pain Relief Cream Extreme	MENTHOL 16%, CAMPHOR 11%	Telebrands Corp	2d54077e-4c8d-aaae-e063-6394a90adb41	2025-02-04	Warnings	Exact identifier application number: M017
Capsaicin External Analgesic	CAPSAICIN	NuCare Pharmaceuticals,Inc.	fd90a67d-d60d-a849-e053-6394a90a2cc8	2025-02-04	Warnings	Exact identifier application number: M017
Rugby Muscle Rub Cream	MUSCLE RUB CREAM	NuCare Pharmaceuticals, Inc.	2d58c15a-5ddb-1b16-e063-6294a90a3fbb	2025-02-04	Warnings	Exact identifier application number: M017
Cetilar	MENTHOL 1.4%	PharmaNutra Usa Corp.	2dd14bd4-b4e1-bc7d-e063-6394a90a1e59	2025-02-04	Warnings	Exact identifier application number: M017
Stopain Extra Strength Continuous	MENTHOL	Troy Manufacturing, Inc.	0d199d39-5b47-4c7f-b83a-757f39aa17b6	2025-02-03	Warnings	Exact identifier application number: M017
TheraCare Pain Relieving Lidocaine Cream	LIDOCAINE HYDROCHLORIDE	Veridian Healthcare	2d42192b-8889-a896-e063-6294a90a4fc8	2025-02-03	Warnings	Exact identifier application number: M017
Tiger Balm Pain Relieving Muscle	METHYL SALICYLATE, MENTHOL, UNSPECIFIED FORM, AND CAMPHOR (SYNTHETIC)	Haw Par Healthcare Ltd.	96b06d3f-8685-4314-ad7d-5d2720f4dde6	2025-02-03	Warnings	Exact identifier application number: M017
Icy Hot Medicated No Mess Applicator	MENTHOL	Chattem, Inc.	4ce2b823-7ef5-4cca-a2d8-2fe781bc958e	2025-02-01	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