Rexall ICE COLD ANALGESIC

Manufacturer: Dolgencorp, LLC
Effective date: 2018-10-04
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:56:58

Label at a glance#

ProductRexall ICE COLD ANALGESIC

Active ingredientMENTHOL

Label structure12 sections

Indications and uses

For the temporary relief of monor aches and pains in muscles and joints associated with: ■ simple backache ■ sprains ■ arthritis ■ strains ■ sports injuries ■ bruises

Dosage and administration

■ clean affected area before applying product ■ adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 2%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of monor aches and pains in muscles and joints associated with:

■ simple backache
■ sprains

■ arthritis

■ strains

■ sports injuries

■ bruises

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

■ with other topical pain relievers

■ with heating pads or heating devices

When using this product

OTC - WHEN USING SECTION

■ do not use in or near 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 last for more than 7 days or clear up and occur again within a few days ■ redness or irritation develops

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

■ clean affected area before applying product ■ adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
311502	menthol 2 % Topical Gel	PSN	1
311502	menthol 0.02 MG/MG Topical Gel	SCD	1
311502	menthol 2 % Topical Gel	SY	1
311502	menthol 2 % topical stick	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55910-088-08	2025-07-29	C162847	48780-1	3b156c62-266f-fb37-e063-e6dba90a4e07	7769ca14-3159-4bfa-e053-2a91aa0a65f1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55910-088-08	Rexall ICE COLD ANALGESIC	227 g in 1 JAR	GEL	227		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55910-088	REXALL ICE COLD ANALGESIC (MENTHOL) GEL [DOLGENCORP, LLC]	1	Legacy NDC, 1 package rows	20181010_7769ca14-3159-4bfa-e053-2a91aa0a65f1.zip

Products#

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

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

Rexall ICE COLD ANALGESIC
Menthol
CARBOXYPOLYMETHYLENE
CUPRIC SULFATE
MAGNESIUM SULFATE, UNSPECIFIED
THYMOL
FD&C BLUE NO. 1
ISOPROPYL ALCOHOL
SODIUM HYDROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55910-088	55910-088-08

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
CARBOXYPOLYMETHYLENE	0A5MM307FC	IACT
CUPRIC SULFATE	LRX7AJ16DT	IACT
MAGNESIUM SULFATE, UNSPECIFIED	DE08037SAB	IACT
THYMOL	3J50XA376E	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
WATER	059QF0KO0R	IACT
MENTHOL	L7T10EIP3A	ACTIB

Source Document#

Source XML

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
7769fdbb-be39-7fc6-e053-2991aa0aa088			7769ca14-3159-4bfa-e053-2a91aa0a65f1	2018-10-04	Warnings	Exact identifier spl id: 7769fdbb-be39-7fc6-e053-2991aa0aa088 spl set id: 7769ca14-3159-4bfa-e053-2a91aa0a65f1

Reported adverse events (FAERS/openFDA)#

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