Eagle Green Balm

Manufacturer: Eagle Indo Pharma, PT
Effective date: 2018-06-15
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:54:08

Label at a glance#

ProductEagle Green Balm

Active ingredientCAMPHOR (SYNTHETIC), MENTHOL

Label structure9 sections

Dosage and administration

for adults and children 2 years of age and older apply to affected area not more than 3 - 4 times daily. Children under 2 years of ageconsult a doctor before use

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Camphor 11%
Menthol 15%

Purpose

OTC - PURPOSE SECTION

Analgesic

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of minor pains and aches of muscles and joints associated with simple backache,arthritis, strains, bruises and sprains

WARNING

WARNINGS SECTION

EXTERNAL USE ONLY

■Do not apply towounds and damaged skin

■Avoid contact with eyes

■Do not bandage tightly

■If condition worsens, or if symptoms persist for more than 7 days discontinue use and consult a doctor

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■Keep this drug out of reach of children

■In case of accidental ingestion seek doctor or Poison Control Center

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

for adults and children 2 years of age and older apply to affected area not more than 3 - 4 times daily. Children under 2 years of ageconsult a doctor before use

Other Information

SPL UNCLASSIFIED SECTION

Do not use otherwise than directed

Keep in a cool dry place

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Vanillin, Clove Oil, petroleum Jelly, Paraffin Wax

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box Label

Products#

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

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

Eagle Green Balm
Camphor Menthol
CLOVE OIL
PARAFFIN
PETROLATUM
CAMPHOR (SYNTHETIC)
MENTHOL
VANILLIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60954-100	60954-100-20, 60954-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CLOVE OIL	578389D6D0	IACT
PARAFFIN	I9O0E3H2ZE	IACT
PETROLATUM	4T6H12BN9U	IACT
CAMPHOR (SYNTHETIC)	5TJD82A1ET	ACTIB
MENTHOL	L7T10EIP3A	ACTIB
VANILLIN	CHI530446X	IACT

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d00c5a74-80de-400d-e053-2995a90af253			6f79b43d-ab35-2b71-e053-2991aa0a1202	2021-11-05	Warnings	Exact identifier spl set id: 6f79b43d-ab35-2b71-e053-2991aa0a1202

Reported adverse events (FAERS/openFDA)#

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