Blue Ice Gel

Manufacturer: Delon Laboratories (1990) Ltd | Laboratoires Delon
Effective date: 2026-06-16
Label type: HUMAN OTC DRUG LABEL
Version: 20
Source: daily-update
Hydrated at: 2026-07-15 00:33:00

Label at a glance#

ProductBlue Ice Analgesic

Active ingredientMENTHOL

Label structure8 sections

Indications and uses

for the temporary relief of minor aches and pains of muscles and joints

Dosage and administration

adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: consult a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 2.0%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of minor aches and pains of muscles and joints

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes
do not apply to wounds or damaged skin
do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens
symptoms persist for more than 7 days or clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
children under 2 years of age: consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

ammonium hydroxide, carbomer, FD&C blue no. 1, isopropyl alcohol, magnesium sulfate, sodium hydroxide, thymol, water

Delon 8oz (227g)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Delon Blue Ice Analgesic Gel 8oz

Penetro 227g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Penetro Blue Ice Analgesic Gel

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 Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Menthol	ACTIVE INGREDIENT	L7T10EIP3A	5
Menthol	ACTIVE MOIETY	L7T10EIP3A	5

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

Blue Ice Analgesic
Menthol
THYMOL
AMMONIA
SODIUM HYDROXIDE
MAGNESIUM SULFATE HEPTAHYDRATE
CARBOMER 934
FD&C BLUE NO. 1
WATER
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
61734-021	61734-021-01, 61734-021-02, 61734-021-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
THYMOL	3J50XA376E	IACT
AMMONIA	5138Q19F1X	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
MAGNESIUM SULFATE HEPTAHYDRATE	SK47B8698T	IACT
CARBOMER 934	Z135WT9208	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
MENTHOL	L7T10EIP3A	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
19	2025-10-16	full-release	2026-06-01 01:39:16
18	2025-03-11	full-release	2026-06-01 00:56:58

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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Blue Ice Analgesic	MENTHOL	Delon Laboratories (1990) Ltd	184ed488-6e62-40c6-bb71-1d523280fd6b	2026-06-16	Warnings	Exact identifier ndc (package): 61734-021-02 ndc (package): 61734-021-03 ndc (package): 61734-021-01 ndc (product): 61734-021 ndc11 (package): 61734002102 ndc11 (package): 61734002103 ndc11 (package): 61734002101 spl id: 546439e4-4be6-7792-e063-6394a90a18f9 spl set id: 184ed488-6e62-40c6-bb71-1d523280fd6b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.