FDA.reportPublic FDA data

Lip Balm Cherry Cola Flavored

Manufacturer
Webb Business Promotions
Effective date
2020-04-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:35:09

Label at a glance#

ProductLip Balm Cherry Cola Flavored
Active ingredientOCTINOXATE, OCTISALATE, OXYBENZONE
Label structure7 sections

Dosage and administration

Apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating Reapply every 2 hours Children under 6 months : Ask a doctor

Storage and handling

Protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Purpose

Sun Screen

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Octinoxate .08%

Octisalate .02%

Benzophenone .03%

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Hydrogenated Soybean Oil, Sunflower Oil, Yellow Bees Wax Pearls, Cocoa Butter, Shea Butter, Vitamin E, Aloe Vera Gel, Cherry Cola Flavoring.

Warnings

WARNINGS SECTION

  • Skin Cancer/Skin Aging Alert: Spending too much time in the sun increases your risk of skin cancer and early skin aging. This product has been shown to only help prevent sunburn, not skin cancer or early skin aging.
  • For external use only.
  • Do not use on damaged or broken skin.
  • Stop use and ask doctor if rash occurs.
  • When using this product keep out of eyes.
  • Keep out of reach of children. If swallowed get medical help or contact posion control center right away.

Directions

INTENDED USE OF THE DEVICE

  • Apply liberally 15 minutes before sun exposure
  • Use a water resistant sunscreen if swimming or sweating
  • Reapply every 2 hours
  • Children under 6 months : Ask a doctor

Storage and Handling Information

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun

SPF 15 NATURAL BEESWAX LIP BALM CHERRY COLA FLAVORED

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cherry ColaCherry Cola

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70445-20570445-205-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WHITE WAX7G1J5DA97FIACT
SUNFLOWER OIL3W1JG795YIIACT
HYDROGENATED SOYBEAN OILA2M91M918CIACT
COCOA BUTTER512OYT1CRRIACT
SHEA BUTTERK49155WL9YIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
OXYBENZONE95OOS7VE0YACTIB

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
b79e425f-454e-db72-e053-2995a90a82b040b7aade-3f3f-21d5-e054-00144ff88e882020-12-29WarningsExact identifier
spl set id: 40b7aade-3f3f-21d5-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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