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Drug Facts

Manufacturer
ONEST LIMITED
Effective date
2026-09-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-03 00:02:03

Label at a glance#

ProductArctic Ice Pain Relieving Gel
Active ingredientMENTHOL
Label structure6 sections

Indications and uses

Temporarily relieves: Minor muscle aches and pains

Dosage and administration

For the temporary relief of minor muscle aches and pains. See important warnings under "When using this product". Not for use on children under 2 years of age. Adults & children 2 years & older: Apply liberally to painful area and massage until gel is absorbed into the skin. Repeat 3 to 4 times daily.

Label contents#

Full prescribing information#

Active Ingredient            Purpose

OTC - ACTIVE INGREDIENT SECTION

Menthol, 1.25%        Topical analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves:

  • Minor muscle aches and pains

Warnings

WARNINGS SECTION

For external use only. Avoid contact with eyes.

  • Ask a doctor before use if you have a cough associated with:
  • Smoking
  • Excessive phlegm
  • Asthma
  • Emphysema
  • Persistent or chronic cough

When using this product, do not:

  • Heat, microwave, or add to hot water or any container where heating water may cause splattering and result in burns
  • Use in eyes or directly on mucous membranes
  • Take by mouth or place in nostrils
  • Apply to wounds or damaged skin
  • Bandage skin

Consult a doctor and discontinue Use:

  • If condition worsens, persists more than 1 week or tends to recur.

Keep out of reach of children.

  • In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

For the temporary relief of minor muscle aches and pains. See important warnings under "When using this product".

  • Not for use on children under 2 years of age.
  • Adults & children 2 years & older: Apply liberally to painful area and massage until gel is absorbed into the skin. Repeat 3 to 4 times daily.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Ethyl Alcohol, Carbomer, Camphor, Sodium Hydroxide, FD&C Blue 1, Methylchloroisothiazolinone, Methylisothiazolinone

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87510-00687510-006-01

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
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
SODIUM HYDROXIDE55X04QC32IIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-08-11daily-update2026-08-18 02:03:06

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
58c4e4f3-b9ec-ed2a-e063-6394a90af35ac63ef7a5-d649-4fba-9361-d37f1150e21d2026-08-11WarningsExact identifier
spl set id: c63ef7a5-d649-4fba-9361-d37f1150e21d

Reported adverse events (FAERS/openFDA)#

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