OTC - ACTIVE INGREDIENT SECTION
Methyl salicylate
I-Menthol
ZENOL COOL
- Manufacturer
- Lydia Co., Ltd.
- Effective date
- 2023-07-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:27:11
Label at a glance#
ProductZENOL COOL
Active ingredientLEVOMENTHOL, METHYL SALICYLATE
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
Kaolin,Zine Oxide,Titanium Oxide,Galatin,Glycerin,Liquid Paraffin,Polybutene,Sodium Polyacrylate,Rubber Latex,Purified Water
OTC - PURPOSE SECTION
For temporary relief of minor aches & pains of muscles & joints Associated with:
• Arthritis •Simple backache •Strains •Bruises •Sprains
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
keep out of reach of the children
INDICATIONS & USAGE SECTION
Adults and children 12 years of age and over:
•Clean and dry affected area •Remove patch from film
•Apply to affected area not more than 3 to 4 times daily
•Remove patch from the skin after at most 8-hour application
Children under 12 years of age:
WARNINGS SECTION
use only as directed
do not bandage tightly or use with a healing pad
avoid contact with the eyes and mucous membranes
do not apply to wounds or damaged skin
DOSAGE & ADMINISTRATION SECTION
for external use only
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- ZENOL COOL
- Methyl salicylate, l-menthol
- LEVOMENTHOL
- WATER
- KAOLIN
- METHYL SALICYLATE
- SALICYLIC ACID
- GLYCERIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72988-0026 | 72988-0026-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| LEVOMENTHOL | BZ1R15MTK7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| KAOLIN | 24H4NWX5CO | IACT |
| METHYL SALICYLATE | LAV5U5022Y | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 297336ec-7729-27d5-e063-6294a90afe2a | ce8817f1-4589-56df-e053-2a95a90a3bcd | 2024-12-17 | Warnings | ce8817f1-4589-56df-e053-2a95a90a3bcd |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.