Ear Pain MD - Pain Relief Drops

Manufacturer: Eosera Inc
Effective date: 2020-01-21
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 23:45:13

Label at a glance#

ProductEar Pain MD

Active ingredientLIDOCAINE HYDROCHLORIDE

Label structure7 sections

Indications and uses

For the temporary relief of pain

Dosage and administration

Consult your doctor before use. Adults and children 2 years of age and older: Apply to affected area not more than 3-4 times daily or as directed by your doctor. Children under 2 years of age: consult a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine Hydrochloride - 4%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of pain

Warnings:

WARNINGS SECTION

For external use only
Do not ingest
Avoid contact with eyes
If conditions worsen, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.
Do not use in large quantities, particularly over raw surfaces or blistered areas
Do not use if you are allergic to any ingredient in this product

Directions

DOSAGE & ADMINISTRATION SECTION

Consult your doctor before use. Adults and children 2 years of age and older: Apply to affected area not more than 3-4 times daily or as directed by your doctor.

Children under 2 years of age: consult a doctor

Other Information

OTHER SAFETY INFORMATION

Store at room temperature (20-25^o C, 68-77^o F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe barbadensis (Aloe), Glycerin, Propylene glycol, Benzalkonium chloride

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package label

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Ear Pain MD
Pain Relief Drops
LIDOCAINE HYDROCHLORIDE
LIDOCAINE
ALOE VERA LEAF
Glycerin
Propylene Glycol
BENZALKONIUM CHLORIDE
Water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72429-0070	72429-0070-6

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
LIDOCAINE HYDROCHLORIDE	V13007Z41A	ACTIR
ALOE VERA LEAF	ZY81Z83H0X	IACT
Glycerin	PDC6A3C0OX	IACT
Propylene Glycol	6DC9Q167V3	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	IACT
Water	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
6039263b-9d02-4dbe-ad6e-af331ba8c4c2			ae6e58fb-5a81-4ccf-ac9f-eabc1f4d3d79	2021-06-25	Warnings	Exact identifier spl set id: ae6e58fb-5a81-4ccf-ac9f-eabc1f4d3d79

Reported adverse events (FAERS/openFDA)#

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