Zenol Double ACTION

Manufacturer
Lydia Co., Ltd.
Effective date
2024-10-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:50:38

Label at a glance#

ProductZenol Double ACTION
Active ingredientLEVOMENTHOL, CAMPHOR (SYNTHETIC), METHYL SALICYLATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Methyl salicylate

I-Menthol

dl-camphor

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

please see the Drug Facts label attached

WARNINGS SECTION

please see the Drug Facts label attached

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72988-004272988-0042-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2973314f-67f6-9466-e063-6394a90a2d5825d26e62-a184-cbed-e063-6294a90afc4f2024-12-17WarningsExact identifier
spl set id: 25d26e62-a184-cbed-e063-6294a90afc4f

Reported adverse events (FAERS/openFDA)#

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