Ice Blue Pain Alleviating Rub

Manufacturer
Lemisol Corporation | Cosmetics & Cleaners International, LLC. DBA C&C Industries
Effective date
2022-08-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:43:42

Label at a glance#

ProductIce Blue Pain Alleviating Rub
Active ingredientMENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)
Label structure9 sections

Dosage and administration

Apply generously to affected area Massage until gel is completely absorbed by skin. Repeat as necessary

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate8%

Menthol 5.0%

Camphor 3.0%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Topical analgesic

Topical analgesic

INDICATIONS & USAGE SECTION

Uses provides temporary relief of minor aches and pains in muscles and joints associated with

  • arthritis
  • simple backache
  • muscle strains
  • sprains
  • bruises
  • cramps

Warnings:

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product use only as directed

  • do not bandage or apply heating pads
  • do not apply to wounds or damaged skin
  • avoid contact with eyes and mucous membranes

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • irritation develops
  • symptoms persist for more than 8 days or clear up and return

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years:

SPL UNCLASSIFIED SECTION

Apply generously to affected area

Massage until gel is completely absorbed by skin. Repeat as necessary

Children under 12 years: ask a doctor before use

OTC - ASK DOCTOR SECTION

Inactive Ingredients

INACTIVE INGREDIENT SECTION

DMDM Hydantoin, Eucalyptus Globulus Leaf Oil, FD&C Blue No 1, Glycerin, Isopropyl Alcohol, PEG-40 Hydrogenated Castor Oil, Purified Water.

Principal Display Panel – 8 oz Spray Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Greaseless

SIN GRASA

Rx
Rysell®

ICE
BLUE®
FORTE

  • PAIN ALLEVIATING RUB
  • ALIVIO RÁPIDO DEL DOLOR

Analgesic/ Analgésico

SPRAY

Net Wt. 4 Oz. (118.2 g)e

Principal Display Panel – 8 oz Spray Label
Principal Display Panel – 8 oz Spray Label

Principal Display Panel – 8 oz Gel Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Greaseless

SIN GRASA

Rx
Rysell®

ICE
BLUE®

Analgesic/ Analgésico

Gel

  • PAIN ALLEVIATING RUB
  • ALIVIO RÁPIDO DEL DOLOR

Net Wt. 8 Oz. (226.7 g)e

Principal Display Panel – 8 oz Gel Label
Principal Display Panel – 8 oz Gel Label

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82988-101ICE BLUE PAIN ALLEVIATING RUB (MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)) GEL ICE BLUE PAIN ALLEVIATING RUB (MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)) SPRAY [LEMISOL CORPORATION]1Legacy NDC20221221_0238f4aa-6f40-489a-9a09-a6ba2d8080b5.zip
82988-102ICE BLUE PAIN ALLEVIATING RUB (MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)) GEL ICE BLUE PAIN ALLEVIATING RUB (MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)) SPRAY [LEMISOL CORPORATION]1Legacy NDC20221221_0238f4aa-6f40-489a-9a09-a6ba2d8080b5.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82988-10182988-101-08, 82988-101-16
82988-10282988-102-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c1a94696-f852-4c09-bc96-c3154b9c59440238f4aa-6f40-489a-9a09-a6ba2d8080b52026-04-03WarningsExact identifier
spl set id: 0238f4aa-6f40-489a-9a09-a6ba2d8080b5

Reported adverse events (FAERS/openFDA)#

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