Eagle Balm

Manufacturer
Anhing Corporation
Effective date
2019-04-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:25:12

Label at a glance#

ProductEagle Balm
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure11 sections

Indications and uses

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

Dosage and administration

■ Adults and children 12 years of age: apply to affected area not more than 3 - 4 times daily. ■children under 12 years of age, consult a doctor before using

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 15%

Camphor 11%

Purpose

OTC - PURPOSE SECTION

External Analgesic

External Analgesic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For External Use Only

When using this product

OTC - WHEN USING SECTION

■ Avoid getting itno the eyes or on mucous membranes ■do not apply to wounds or damaged skin ■do not bandage tightly or use with a heating pad ■do not use otherwise than as directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

■Conditions worsens ■symptoms persist for more than 7 days or clear up and occur again within a few days ■redness is present

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Adults and children 12 years of age: apply to affected area not more than 3 - 4 times daily. ■children under 12 years of age, consult a doctor before using

Other Information

SPL UNCLASSIFIED SECTION

■ Store in a a cool, dry place

Inactive Ingredients

INACTIVE INGREDIENT SECTION

fragrance, paraffin, peppermint oil, petrolatum

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51398-01051398-010-19, 51398-010-01

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
b69da782-84b2-40cc-e053-2995a90ac83787625838-5cb1-e91d-e053-2995a90a4d412020-12-16WarningsExact identifier
spl set id: 87625838-5cb1-e91d-e053-2995a90a4d41

Reported adverse events (FAERS/openFDA)#

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