FDA.reportPublic FDA data

EZ+ WOUNDCARE Pain Relieving and First Aid Antiseptic Ointment

Manufacturer
EZ Medical Solutions LLC
Effective date
2021-12-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:23:13

Label at a glance#

ProductEZ WOUNDCARE Pain Relieving and First Aid Antiseptic
Active ingredientBENZOCAINE, POVIDONE-IODINE
Label structure9 sections

Indications and uses

First aid to help prevent infection in minor cuts, scrapes, and burns. For the temporary relief of pain in minor cuts, scrapes, and burns.

Dosage and administration

Clean the affected area.  Adults and children 2 years of age and older: Apply a small amount of this product on the affected area 1 to 3 times daily May be covered by a sterile bandage. Children under 2 years of age: Consult a doctor.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Banzocaine 5.0%

Povidone Iodine 7.0%

Purposes

OTC - PURPOSE SECTION

Pain Relieving

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • First aid to help prevent infection in minor cuts, scrapes, and burns.
  • For the temporary relief of pain in minor cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

in the eyes.

When using this product:

OTC - WHEN USING SECTION

  • avoid contact with the eyes.
  • do not apply to large areas of the body.
  • in case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens, or if symptoms persist for more than 7 days or clean up and occur again within a few days.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean the affected area. 
  • Adults and children 2 years of age and older: Apply a small amount of this product on the affected area 1 to 3 times daily
  • May be covered by a sterile bandage.
  • Children under 2 years of age: Consult a doctor.

Other information

SPL UNCLASSIFIED SECTION

  • Store at 59-86°F (15-30°C)
  • Avoid heat and direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Calcium carbonate, deionized water, glycerin, sucrose, methylparaben, xanthan gum

Questions or comments?

OTC - QUESTIONS SECTION

520-490-5115

Package Labeling:30g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:90g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57554-13057554-130-01, 57554-130-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALCIUM CARBONATEH0G9379FGKIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
SUCROSEC151H8M554IACT
METHYLPARABENA2I8C7HI9TIACT
XANTHAN GUMTTV12P4NEEIACT
BENZOCAINEU3RSY48JW5ACTIB
POVIDONE-IODINE85H0HZU99MACTIM

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
d31fed1c-63d0-9abe-e053-2995a90acfcab2954e2d-9a62-75b3-e053-2995a90a42dc2021-12-14WarningsExact identifier
spl id: d31fed1c-63d0-9abe-e053-2995a90acfca
spl set id: b2954e2d-9a62-75b3-e053-2995a90a42dc

Reported adverse events (FAERS/openFDA)#

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