ARCTIC ICE

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date
2023-10-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:24:00

Label at a glance#

ProductARCTIC ICE
Active ingredientMENTHOL
Label structure10 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:

OTC - ACTIVE INGREDIENT SECTION

Menthol, 1.25%

Purpose

OTC - PURPOSE SECTION

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 cough associated with smoking, excessive phlegm, asthma, emphysema, persistent or chronic cough.

When using this product, do not:

OTC - WHEN USING SECTION

heat

microwave

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:

OTC - STOP USE SECTION

if condition worsens, persists for more than 1 week or tends to recur.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Blue 1, Camphor, Carbomer, Ethyl Alcohol, Methylchoroisothiazolinone, Methylisothiazolinone, Sodium Hydroxide, Water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-20676176-206-01

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32023-05-01daily-update2026-09-15 03:02:25

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
07f5dddd-1fbc-1609-e063-6394a90ab7ff07f5ec88-fbdf-6801-e063-6294a90ab8662023-10-01WarningsExact identifier
spl id: 07f5dddd-1fbc-1609-e063-6394a90ab7ff
spl set id: 07f5ec88-fbdf-6801-e063-6294a90ab866

Reported adverse events (FAERS/openFDA)#

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