Signature Care Maximum Strength Cold Sore Treatment

Manufacturer
Safeway
Effective date
2021-03-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:49:11

Label at a glance#

ProductSignature Care Maximum Strength Cold Sore Treatment
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, PETROLATUM, PHENOL
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 and comments?

OTC - QUESTIONS SECTION

Call us toll-free at 1-877-242-3234 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.

Cold Sore Tube card PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Maximum Strength

Camphor 3.00%, Menthol 1.00%, Phenol 1.50%, White Petrolatum 89.20%

Cold Sore Treatment

Medicated

Temporary Relief of Pain and Discomfort!

Paraben Free with Tea Tree Oil

Works on contact

Applies clear

Phthalate free

Sulfate Free

Medicated

Cold Sore/Fever Blister Treatment & Skin Protectant

NET WT 0.07 OZ (2 g)

cold-sore-treatment
cold-sore-treatment

FDA-Initiated Inactive NDC Indexing#

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
21130-41821130-418-01

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

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6e639f1d-0624-4ca3-9363-e53fdba1b55597ba7de3-93d9-9e3f-e053-2a95a90a94642022-09-13WarningsExact identifier
spl set id: 97ba7de3-93d9-9e3f-e053-2a95a90a9464

Reported adverse events (FAERS/openFDA)#

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