Sno Swedish Arctic Gel Relief

Manufacturer
Natumin Pharma AB
Effective date
2016-01-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:33

Label at a glance#

ProductSno Swedish Arctic Gel Relief
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM
Label structure11 sections

Indications and uses

temporarily relieves minor pain associated with simple backache muscle strains sprains bruises

Dosage and administration

adults and children over 12 years: apply a thin layer to affected area massage into painful area until thoroughly absorbed into skin repeat as necessary, but no more than 3 to 4 times daily, allowing a minimum of 2-3 hours between applications. After applying, wash hands with soap and water. Children 12 years or younger: ask a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 2.2%

Menthol 3.6%

Purpose

DOSAGE & ADMINISTRATION SECTION

Topical Analgesic

Uses

OTC - PURPOSE SECTION

temporarily relieves minor pain associated with

  • simple backache
  • muscle strains
  • sprains
  • bruises

Warning

WARNINGS SECTION

For external use only

When using this product

  • use only as directed
  • read and follow all directions and warnings on this label
  • rare cases of serious burns have been reported with products of this type
  • do not bandage tightly or apply local heat (such as heating pads) or medicated patches to the area of use
  • avoid contact with eyes and mucous membranes
  • do not apply to wounds or damaged, broken, or irritated skin
  • a transient burning sensation may occur upon application but generally disappears in several days

Stop use and ask doctor if

OTC - STOP USE SECTION

  • Condition worsens
  • redness is present
  • irritation develops
  • symptoms persis for more than 7 days or clear up and occur again within a few days
  • you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

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

If swallowed, get medical help or contact a Poison Control Center right away

Directions

INDICATIONS & USAGE SECTION

adults and children over 12 years:

apply a thin layer to affected area

massage into painful area until thoroughly absorbed into skin

repeat as necessary, but no more than 3 to 4 times daily, allowing a minimum of 2-3 hours between applications.

After applying, wash hands with soap and water.

Children 12 years or younger: ask a doctor

Other Information

INSTRUCTIONS FOR USE SECTION

Store at 68-77°F (20-25°C)

Protect from excessive moisture

Inactive Ingredients

INACTIVE INGREDIENT SECTION

ammonium acryloyldimethyltaurate/ VP copolymer

ethylhexylglycerin

glycerin

isostearyl isostearate

PEG-40 hydrogenated castor oil

phenoxyethanol

propylene glycol

sodium hydroxide

water

Principle Display Panel-100g tube carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sno Swedish Arctic Gel Relief CartonSno Swedish Arctic Gel Relief Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1729314camphor 2.2 % / menthol 3.6 % Topical GelPSN1
1729314camphor 0.022 MG/MG / menthol 0.036 MG/MG Topical GelSCD1
1729314camphor 2.2 % / menthol 3.6 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70316-330-022020-01-31C16284748780-19d75b9d0-8122-f424-e053-dadaa90a57ce28973151-755f-6cd8-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70316-330-02Sno Swedish Arctic Gel Relief1 in 1 CARTONGEL11
70316-330-02Sno Swedish Arctic Gel Relief100 g in 1 TUBEGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70316-330SNO SWEDISH ARCTIC GEL RELIEF (CAMPHOR, MENTHOL) GEL [NATUMIN PHARMA AB]1Legacy NDC, 2 package rows20160105_28973151-755f-6cd8-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70316-33070316-330-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
28973151-7560-6cd8-e054-00144ff88e8828973151-755f-6cd8-e054-00144ff88e882016-01-05WarningsExact identifier
spl id: 28973151-7560-6cd8-e054-00144ff88e88
spl set id: 28973151-755f-6cd8-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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