FDA.reportPublic FDA data

Arctic Blast Pain Releiving Drops

Manufacturer
Nutriomo Labs Pte, Ltd
Effective date
2025-03-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:56:55

Label at a glance#

ProductArctic Blast Pain Releiving
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure8 sections

Dosage and administration

For adults: Apply to affected area no more than 3 to 4 times daily.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 10.00%

Camphor 3.00%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Indications:

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of the muscles and joints associated with: • arthritis • sprains • strains • bruises • simple backache

Warnings

WARNINGS SECTION

  • For external use only.
  • Use only as directed.

Flammable

  • Keep away from fire, flame, sparks and heated surfaces.
  • Tighten cap firmly.

Stop use and ask doctor if

OTC - STOP USE SECTION

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

If pregnant or breat-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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

For adults: Apply to affected area no more than 3 to 4 times daily.

Other Information

SPL UNCLASSIFIED SECTION

  • Store product at room temperature
  • Do not use if printed safety seal on cap is broken or missing

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Calendula Officinalis Extract, Dimethyl Sulfoxide (DMSO), Emu Oil, Ethylhexylglycerin, Glycerin, Hypericum Perforatum (St. John's Wort), Isopropyl Alcohol, Methyl Salicylate, Olea Europaea (Olive) Oil, Phenoxyethanol, Polysorbate-20, Propylene Glycol, SD-Alcohol 40B.

Questions?

OTC - QUESTIONS SECTION

Call 1-800-856-5587

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0Label0

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1987413camphor 3 % / menthol 10 % Topical SolutionPSN3
1987413camphor 30 MG/ML / menthol 100 MG/ML Topical SolutionSCD3
1987413camphor 3 % / menthol 10 % Topical SolutionSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71856-176-01Arctic Blast Pain Releiving30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71856-176ARCTIC BLAST PAIN RELEIVING (MENTHOL, CAMPHOR (SYNTHETIC)) LIQUID [NUTRIOMO LABS PTE, LTD]3Current NDC, Legacy NDC, 1 package rows20250311_d5e7d26d-4f63-4b7b-a173-fe3a794c8459.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71856-17671856-176-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
DIMETHYL SULFOXIDEYOW8V9698HIACT
EMU OIL344821WD61IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
HYPERICUM PERFORATUM WHOLEXK4IUX8MNBIACT
ISOPROPYL ALCOHOLND2M416302IACT
METHYL SALICYLATELAV5U5022YIACT
OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLESXO45V955LTIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
MENTHOLL7T10EIP3AACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB

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
Arctic Blast Pain ReleivingMENTHOL, CAMPHOR (SYNTHETIC)Nutriomo Labs Pte, Ltdd5e7d26d-4f63-4b7b-a173-fe3a794c84592025-03-10WarningsExact identifier
ndc (package): 71856-176-01
ndc (product): 71856-176
ndc11 (package): 71856017601
spl id: 2ffc226d-1051-58a4-e063-6294a90a349b
spl set id: d5e7d26d-4f63-4b7b-a173-fe3a794c8459

Reported adverse events (FAERS/openFDA)#

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