Mineral Ice Extreme Dry Stick

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
Mineral Ice Extreme Dry Stick
Generic name
MENTHOL
Manufacturer
Carlin Consumer Health LLC
Product type
HUMAN OTC DRUG
SPL set ID
4f81be91-92e5-1205-e063-6394a90a6e82
SPL ID
53464550-4096-d2cb-e063-6394a90aa89e
Version
2
Effective date
2026-06-02
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:28:57
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use • with other topical pain relievers • with heating pads or heating devices When using this product • Avoid contact with eyes • do not apply to wounds or damaged skin • do not bandage tightly Stop use and ask a doctor if • condition worsens • symptoms last more than 7 days or clear up and occur again within a few days If preganant or breast feeding , as a health professional before use. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Reported adverse events (FAERS/openFDA)#

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