RELISPRAY NATURAL PAIN RELIEF

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
RELISPRAY NATURAL PAIN RELIEF
Generic name
MENTHOL
Manufacturer
Midas-Care Pharmaceuticals, Pvt. Ltd
Product type
HUMAN OTC DRUG
SPL set ID
adc8a43c-19a1-4eb3-9820-b63f7b5e91ea
SPL ID
e0528d1b-37dc-4576-bfd5-18705d517933
Version
1
Effective date
2025-10-30
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 05:54:39
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. Flammable: Keep away from excessive heat or open flame. Do not store at temperature above 120°F. Contents under pressure. Do not puncture or Incinerate. Ask a doctor before use if you have: Sensitive skin. When using this product • Use only as directed. • Avoid contact with the eyes or on mucous membranes. • Do not apply to wounds or damaged skin. • Do not apply to irritated skin or if excessive irritation develops. • Do not bandage. • Do not use with heating pad or device. Stop use and ask a doctor if • You experience pain, swelling or blistering of the skin. • Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. • Arthritic pain persists for more than 10 days, or redness is present If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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