eos Medicated Pain Relieving Lip Balm

Manufacturer
eos Products LLC
Effective date
2015-11-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:16

Label at a glance#

Producteos Medicated Pain Relieving Lip Balm
Active ingredientPHENOL
Label structure13 sections

Indications and uses

For the temporary relief of pain associated with cold sores.

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - PURPOSE SECTION

Active Ingredients        Purpose

Phenol 0.68%               External Analgesic  

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of pain associated with cold sores.

Warnings

WARNINGS SECTION

For external use only

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

If condition worsens, 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
Children under 2 years of age: consult a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Beeswax, Simmondsia Chinensis (Jojoba) Seed Oil, Camellia Oleifera Seed Oil, Butyrospermum Parkii (Shea) Butter, Cucurbita Pepo (Pumpkin) Seed Oil, Flavor (Aroma), Euterpe Oleracea Fruit Extract, Zingiber Officinale (Ginger) Root Extract, Punica Granatum Seed Oil, Camellia Sinensis Leaf Extract, Tocopherol, Stevia Rebaudiana Leaf/Stem Extract, Glycine Soja (Soybean) Oil, Helianthus Annuus (Sunflower) Seed Oil.

Other Information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

Questions or Comments

OTC - QUESTIONS SECTION

(866) 547-4367

Principle Display Panel - 0.25 oz BLISTER PACK

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

eos 

Medicated Pain Relieving 

Lip Balm 

Tangerine

Net wt. 0.25 oz (7 g)

eos medicated lip balm blistereos medicated lip balm blister

Principle Display Panel - 0.25 oz CELLO PACK

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

eos
Medicated Pain Relieving
Lip Balm
Tangerine
Net wt. 0.25 oz (7 g)

eos medicated lip balm celloeos medicated lip balm cello

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70170-0003-12020-01-31C16284748780-19d75b9d0-534a-f424-e053-dadaa90a57ceeos Medicated Pain Relieving Lip Balm
70170-0004-12020-01-31C16284748780-19d75b9d0-534a-f424-e053-dadaa90a57ceeos Medicated Pain Relieving Lip Balm

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70170-0003-1eos Medicated Pain Relieving Lip Balm1 in 1 PACKAGESTICK11
70170-0003-1eos Medicated Pain Relieving Lip Balm7 g in 1 BLISTER PACKSTICK71
70170-0004-1eos Medicated Pain Relieving Lip Balm1 in 1 PACKAGESTICK11
70170-0004-1eos Medicated Pain Relieving Lip Balm7 g in 1 CELLO PACKSTICK71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70170-0003EOS MEDICATED PAIN RELIEVING LIP BALM (PHENOL) STICK [EOS PRODUCTS LLC]1Legacy NDC, 2 package rows20151203_b1a66915-1711-4ce3-aafe-3dfb345d676d.zip
70170-0004EOS MEDICATED PAIN RELIEVING LIP BALM (PHENOL) STICK [EOS PRODUCTS LLC]1Legacy NDC, 2 package rows20151203_b1a66915-1711-4ce3-aafe-3dfb345d676d.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70170-000370170-0003-1
70170-000470170-0004-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c1d62007-a05c-4b74-8e55-785550ca99e0b1a66915-1711-4ce3-aafe-3dfb345d676d2015-11-02WarningsExact identifier
spl id: c1d62007-a05c-4b74-8e55-785550ca99e0
spl set id: b1a66915-1711-4ce3-aafe-3dfb345d676d

Reported adverse events (FAERS/openFDA)#

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