FDA.reportPublic FDA data

RAMEDICA

Manufacturer
Ramedicare Sdn. Bhd.
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:12:42

Label at a glance#

ProductRAMEDICA
Active ingredientCAMPHOR (NATURAL), EUCALYPTUS OIL, MENTHOL, PEPPERMINT OIL
Label structure9 sections

Indications and uses

For temporary relief of the minor aches and pains in muscles and joints related to rheumatism, arthritis, backaches, strains, sprains, sports and other minor injuries.

Dosage and administration

For adults and children over 12, rub well on the affected area. Repeat 3 to 4 times daily For children 12 years of age or younger, consult a doctor before use.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor

Eucalyptus Oil

Menthol

Peppermint oil

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Borneol 1%
Cassia Oil 1%
Cinnamon Leaf Oil 6%
Citronella Oil 6%
Clove Oil, Nutmeg Oil 6%
Paraffin Wax 17%
Petroleum Jelly 21%

Directions

DOSAGE & ADMINISTRATION SECTION

For adults and children over 12, rub well on the affected area. Repeat 3 to 4 times daily

For children 12 years of age or younger, consult a doctor before use.

Directions

DOSAGE & ADMINISTRATION SECTION

For adults and children over 12, rub well on the affected area. Repeat 3 to 4 times daily

For children 12 years of age or younger, consult a doctor before use.

Warnings

WARNINGS SECTION

WARNINGS: For external use only. When using this product: Discontinue use if excessive irritation of the skin develops. Avoid contact with eyes and mucus membranes. Do not bandage tightly. Do not use with heating pad.

Stop use and ask a doctor if:
▪ Condition worsens. ▪ Severe skin irritation occurs. ▪ Pain persists for more than seven days. ▪ Pain clears up and the recurs within a few days.

If pregnant or breast-feeding, ask a health care professional before use.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control immediately.

Uses

INDICATIONS & USAGE SECTION

For temporary relief of the minor aches and pains in muscles and joints related to rheumatism, arthritis, backaches, strains, sprains, sports and other minor injuries.

Container Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product labelProduct label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66059-0002-12021-02-19C16284748780-1ba0f9c33-3e9a-a910-e053-dadaa90a0b850d988182-d435-465d-b99b-5eeee7b76e74
66059-0002-12021-01-29C16284748780-1ba0f9c33-3e9a-a910-e053-dadaa90a0b850d988182-d435-465d-b99b-5eeee7b76e74

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66059-000266059-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
BORNEOLM89NIB437XIACT
PADANG CASSIA OIL0E15252LIWIACT
CLOVE OIL578389D6D0IACT
CINNAMON LEAF OILS92U8SQ71VIACT
CITRONELLA OILQYO8Q067D0IACT
NUTMEG OILZ1CLM48948IACT
PETROLATUM4T6H12BN9UIACT
PARAFFINI9O0E3H2ZEIACT
CAMPHOR (NATURAL)N20HL7Q941ACTIB
EUCALYPTUS OIL2R04ONI662ACTIB
MENTHOLL7T10EIP3AACTIB
PEPPERMINT OILAV092KU4JHACTIB

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
d60a3e9d-e881-3b19-e053-2995a90a3e8d0d988182-d435-465d-b99b-5eeee7b76e742022-01-20WarningsExact identifier
spl id: d60a3e9d-e881-3b19-e053-2995a90a3e8d
spl set id: 0d988182-d435-465d-b99b-5eeee7b76e74

Reported adverse events (FAERS/openFDA)#

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