Maximum Strength Cold Sore Treatment

Manufacturer
Target Corporation
Effective date
2024-11-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:49:23

Label at a glance#

ProductMaximum Strength Cold Sore Treatment
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, PHENOL, PETROLATUM
Label structure9 sections

Indications and uses

• For treatment of cold sores/fever blisters on the face or lips • Temporarily relieves the symptoms of itching and pain associated with cold sores/fever blisters • Temporarily protects minor cuts, scrapes, burns, and sores • Helps prevent and temporarily protects chapped or cracked skin and lips

Dosage and administration

• Clean the affected area • Apply a small amount of this product to the affected area 1 to 3 times daily • Rub in gently • May be covered with a sterile bandage • Wash hands before and after applying cream • Do not share this product with anyone • Children under 12 years of age: ask a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.00%

Menthol 1.00%

Phenol 1.50%

White Petrolatum 89.20%

Purpose

OTC - PURPOSE SECTION

Cold sore/fever blister treatment

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

  • For treatment of cold sores/fever blisters on the face or lips
  • Temporarily relieves the symptoms of itching and pain associated with cold sores/fever blisters
  • Temporarily protects minor cuts, scrapes, burns, and sores
  • Helps prevent and temporarily protects chapped or cracked skin 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

OTC - WHEN USING SECTION

avoid contact with eyes. Use only as directed.

Stop use and consult a doctor if

OTC - STOP USE SECTION

the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean the affected area
  • Apply a small amount of this product to the affected area 1 to 3 times daily
  • Rub in gently
  • May be covered with a sterile bandage
  • Wash hands before and after applying cream
  • Do not share this product with anyone
  • Children under 12 years of age: ask a doctor

Other information

OTHER SAFETY INFORMATION

store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Eucalyptol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Thymol, Tocopheryl Nicotinate

Questions or comments?

OTC - QUESTIONS SECTION

Call us toll-free at 1-800-910-6874 Monday-Friday, 9 a.m. to 5 p.m. EST.

Serious side effects associated with use of this product may be reported to this number.

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

maximum strength

camphor 3.00%, menthol 1.00%, phenol 1.50%, white petrolatum 89.20%

cold sore treatment

cold sore/fever blister treatment and skin protectant

temporary relief of pain and discomfort

works on contact

applies clear

paraben free

NET WT 0.07 OZ (2.0 g)

apply up to 3 times daily

cold-sore-treatmentcold-sore-treatment

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-412-012021-03-16C16284748780-1ba0f9c33-16e9-a910-e053-dadaa90a0b85Cold Sore Treatment – Drug Facts
11673-412-012021-01-29C16284748780-1ba0f9c33-16e9-a910-e053-dadaa90a0b85Cold Sore Treatment – Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-412MAXIMUM STRENGTH COLD SORE TREATMENT (CAMPHOR, MENTHOL, PHENOL, WHITE PETROLATUM) GEL [TARGET CORPORATION]4Legacy NDC20241116_8c638c33-a63b-1c6b-e053-2995a90a41f3.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-41211673-412-01

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ba33c00e-b3aa-413c-8b8c-efa97934506c8c638c33-a63b-1c6b-e053-2995a90a41f32024-11-14WarningsExact identifier
spl id: ba33c00e-b3aa-413c-8b8c-efa97934506c
spl set id: 8c638c33-a63b-1c6b-e053-2995a90a41f3

Reported adverse events (FAERS/openFDA)#

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