Aldamed

Manufacturer
Green Idea s.r.o.
Effective date
2023-11-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:20:58

Label at a glance#

ProductAldamed
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure13 sections

Dosage and administration

apply on the affected area and rub gently till absorbed. Apply up to 3 times daily. do no use on children below the age of 3 years old

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 3%.....................Topical Analgesic

Camphor 3%. .................Topical Analgesic

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

Temporary relief from minor aches and pains of sore muscles and joints associated with arthritis, simple backache, bruises, strains, and sprains.

warnings

WARNINGS SECTION

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

directly on mucous membranes

on open skin wounds or burns

When using this product

OTC - WHEN USING SECTION

do not use it in or near the eyes or mouth.

OTC - ASK DOCTOR SECTION

if pregnant or if you have a cough associated with smoking, excessive phlegm, asthma, emphysema, or persistent or chronic cough.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation, itching, or rash occurs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help, or contact a poison control center immediately at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

apply on the affected area and rub gently till absorbed. Apply up to 3 times daily.

do no use on children below the age of 3 years old

Other information

OTHER SAFETY INFORMATION

Store in a cool, and dry place and avoid freezing and excessive heat

Do not expose the product to the direct sunlight

Inactive ingredient

INACTIVE INGREDIENT SECTION

water, alcohol denat., glycerin, symphytum officinale root extract, aesculus hippocastanum seed extract, eucalyptus globulus leaf oil, abies alba leaf oil, dimethyl sulfone, equisetum arvense extract, mentha piperita oil, magnesium pca, sodium hyaluronate, thymus vulgaris oil, juniperus communis fruit oil, nelumbo nucifera flower water, nymphaea coerulea flower water, arnica montana flower extract, ginkgo biloba leaf extract, hydrolyzed collagen, scutellaria baicalensis extract, pinus pumila twig leaf oil, pinus mugo twig oil, echinacea purpurea extract, agrimonia eupatoria extract, calendula officinalis flower extract, vaccinium myrtillus fruit extract, polygonum bistorta root extract, citrus limon fruit oil, citrus grandis peel oil, rosmarinus officinalis leaf oil, lavandula angustifolia oil, calluna vulgaris extract, ribes nigrum fruit extract, chamomilla recutita flower extract, carbomer, polysorbate 80, phenoxyethanol, sodium hydroxide, ethylhexylglycerin, peg-12 dimethicone

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PainElliminPainEllimin200 mL, NDC: 82810-111-11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82810-111-112024-01-30C16284748780-11030e365-39f1-111a-e063-dadaa90a10e2Green Idea-Herbamedicus PainEllimin Collagen

Products#

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

DailyMed product names page 1 of 2 · 43 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82810-11182810-111-11

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 41 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
1e0ebe7d-b805-b9e2-e063-6294a90af28fe5bca8d2-134e-ff26-e053-2995a90a34882024-07-25WarningsExact identifier
spl set id: e5bca8d2-134e-ff26-e053-2995a90a3488

Reported adverse events (FAERS/openFDA)#

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