Arctic Blast Pain Releiving

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Arctic Blast Pain Releiving
Generic name
MENTHOL, CAMPHOR (SYNTHETIC)
Manufacturer
Nutriomo Labs Pte, Ltd
Product type
HUMAN OTC DRUG
SPL set ID
d5e7d26d-4f63-4b7b-a173-fe3a794c8459
SPL ID
2ffc226d-1051-58a4-e063-6294a90a349b
Version
3
Effective date
2025-03-10
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:55:52
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings 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 condition worsens or symptoms persist for more than 7 days symptoms clear up and occur again within a few days When using this product avoid contact with the eyes do not apply to wounds or damaged skin do not bandage tightly If pregnant or breat-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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