Dona

Manufacturer
Sj Incorporation Ltd | Unexo Life Sciences Private Ltd.
Effective date
2023-11-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:02:36

Label at a glance#

ProductDona
Active ingredientMENTHOL, EUCALYPTUS OIL
Label structure7 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints due to simple back ache, arthritis, strains, and sprains.

Dosage and administration

Dry skin before use. Cut open the foil sachet, remove a patch and peel off the protective paper from the central cut. Tip: Be careful when peeling the protective paper as the patch can stick to itself. Apply adhesive side of the patch where you want the cooling effect. Remove gently using warm water to loosen the adhesive. Discard and replace with a new patch as required.

Label contents#

Full prescribing information#

Drug Facts: Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Mentha Piperita            Menthol               Arial Parts            10%

Eucalyptus Globulus      Eucalyptus Oil      Leaf Oil               5%

Other Ingredients:

INACTIVE INGREDIENT SECTION

Adhesive (Tracaganth Gum Rasin Ester, Guar Gum Rosin Ester)* Naturally derived

Uses:

OTC - PURPOSE SECTION

Temporarily relieves minor aches and pains of muscles and joints due to simple back ache, arthritis, strains, and sprains.

Idications & Usuage

INDICATIONS & USAGE SECTION

Discreet and Comfortables

Warnings: For External Use Only

WARNINGS SECTION

Disclaimer: This product is not intended to diagnose and/or prevent any ailment or disease.

  • Single use only
  • Product patches have not been tested on animals
  • Store below 25 ºC in a dry place, out of sight and reach of children
  • Do not freeze
  • Not recommended for use during pregnancy or for those planning a pregnancy
  • Do not apply to broken, irritated skin or near to eyes
  • Do not use if you have eczema or other skin problems
  • In case of irritation or rash stop using the patch immediately.

If problem persists consult your GP. 

Directions:

DOSAGE & ADMINISTRATION SECTION

  1. Dry skin before use. Cut open the foil sachet, remove a patch and peel off the protective paper from the central cut. Tip: Be careful when peeling the protective paper as the patch can stick to itself.
  2. Apply adhesive side of the patch where you want the cooling effect.
  3. Remove gently using warm water to loosen the adhesive. Discard and replace with a new patch as required.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

frontfront

backback

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2670206eucalyptus oil 5 % / menthol 10 % Medicated PatchPSN1
2670206Eucalyptus oil 0.05 MG/MG / menthol 0.1 MG/MG Medicated PatchSCD1
2670206eucalyptus oil 5 % / menthol 10 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83658-009-012025-01-30C16284748780-12cef2736-a2a0-d83d-e063-dadaa90ab31fDona Monthly Patches Discreet & Comfortables

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83658-009-01Dona5 mg in 1 PACKAGEPATCH51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83658-009DONA (MENTHOL EUCALYPTUS) PATCH [SJ INCORPORATION LTD]11 package rows20231122_75835852-0a8b-480a-90c0-b2009330ea69.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83658-00983658-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
GUAR GUME89I1637KEIACT
MENTHOLL7T10EIP3AACTIB
EUCALYPTUS OIL2R04ONI662ACTIB

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
0aa0788a-fbf5-c975-e063-6394a90a8e0a75835852-0a8b-480a-90c0-b2009330ea692023-11-20WarningsExact identifier
spl id: 0aa0788a-fbf5-c975-e063-6394a90a8e0a
spl set id: 75835852-0a8b-480a-90c0-b2009330ea69

Reported adverse events (FAERS/openFDA)#

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