ZIMS MAX FREEZE LEG CRAMP

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
ZIMS MAX FREEZE LEG CRAMP
Generic name
MENTHOL
Manufacturer
KOBAYASHI Healthcare International, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
7ef03298-6623-4cf4-b21f-74b2ffc11c6e
SPL ID
223b6899-de24-47f9-842b-588689ab1a41
Version
3
Effective date
2023-11-16
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:52
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 Flammable Keep away from fire or flame and heated surfaces Do not use if you are allergic to any ingredient in this product on open wounds, damaged or irritated skin after expiration date When using this product to avoid excess application, press applicator gently against skin do not bandage tightly or cover with wrap or use heating pad or TENS device do not use 1 hour prior to bathing or within 30 minutes after bathing do not use other than as directed avoid contact with eyes or mucous membranes Stop use and ask a doctor if condition worsens rash, itching, redness, or excessive irritation, burning sensation, swelling or blistering of the skin develops symptoms persist for more than 7 days symptoms clear up and occur again within a few days If you are pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children and pets. 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.