FDA.reportPublic FDA data

Good Neighbor Pharmacy Cold Sore Treatment

Manufacturer
Good Neighbor Pharmacy | OraLabs
Effective date
2017-01-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:20:39

Label at a glance#

ProductGood Neighbor Pharmacy Cold Sore Treatment
Active ingredientBENZOCAINE
Label structure8 sections

Indications and uses

For treatment of cold sores/fever blisters on the face and lips

Dosage and administration

Clean the affected Adults and children 2 years of age and older: Apply to affected area not more than 4 times daily Children under 2 years of age: consult a physician Rub in gently – Applies clear Wash hands before and after applying cream Do not share this product with anyone

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine

Purpose

OTC - PURPOSE SECTION

Cold Sore/Fever Blister Treatment/Pain Reliever

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 at 1-800-222-1222.

Uses

INDICATIONS & USAGE SECTION

For treatment of cold sores/fever blisters on the face and lips

Warnings

WARNINGS SECTION

For external use only: Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites or serious burns, consult a physician.

Allergy Alert: Do not use if you are allergic to any of the ingredients in this product.

When using this product avoid contact with eyes. Use only as directed.

Stop use and ask a doctor if the condition gets worse. Do not use longer than 1 week unless directed by a doctor.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected

Adults and children 2 years of age and older: Apply to affected area not more than 4 times daily

Children under 2 years of age: consult a physician

Rub in gently – Applies clear

Wash hands before and after applying cream

Do not share this product with anyone

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Benzyl Alcohol, Docosanol, Mineral Oil, Propylene Glycol, Sucrose Stearate, Tocopherol, Water.

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back of Card
Front and Back of Card

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46122-50146122-501-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
LIGHT MINERAL OILN6K5787QVPIACT
BENZOCAINEU3RSY48JW5ACTIB
DOCOSANOL9G1OE216XYIACT
BENZYL ALCOHOLLKG8494WBHIACT
SUCROSE STEARATE274KW0O50MIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT

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
c36d259c-2edd-45ad-b56b-2183d5baeca612d16d19-2ee6-42e1-a075-6d780aa5a3e92017-01-10WarningsExact identifier
spl set id: 12d16d19-2ee6-42e1-a075-6d780aa5a3e9

Reported adverse events (FAERS/openFDA)#

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