Sunscreen and insect repellent

Manufacturer
Bullfrog Brands, LLC | Prime Enterprises
Effective date
2025-01-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:52:19

Label at a glance#

ProductSunscreen and insect repellent Bull frog
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OCTINOXATE
Label structure14 sections

Indications and uses

helps prevent sunburn

Dosage and administration

apply liberally 15 minutes before sun exposure reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours children under 6 months of age: ask a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%, Octocrylene 5%, Homosalate 10.0%, Octyl methoxycinnamate 7.5%, Octisalate 5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only

Skin Alert • Limiting sun exposure, wearing protective clothing, and using sunscreen may reduce the risk of skin aging,
skin cancer and other harmful effects of the sun

FLAMMABLE:

WARNINGS AND PRECAUTIONS SECTION

• do not use near heat, flame or while smoking

• avoid long term storage above 104°F (40°C)

• do not puncture or incinerate

• contents under pressure

• do not store at temperatures above 120°F (49°C).

OTC - DO NOT USE SECTION

Do not use • on damaged or broken skin.

OTC - WHEN USING SECTION

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

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if • rash occurs.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • reapply:

• after 80 minutes of swimming or sweating

• immediately after towel drying

• at least every 2 hours

  • children under 6 months of age: ask a doctor

Other information

OTHER SAFETY INFORMATION

• Protect the product in this container from excessive heat and direct sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/Octylacrylamide Copolymer, SD Alcohol 40 (47% w/w), AloeBarbadensis Leaf Oil, C12-15 Alkyl Benzoate, Fragrance, Tocopheryl (Vitamin E) Acetate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77714-003-15Sunscreen and insect repellentBull frog156 g in 1 CANAEROSOL, SPRAY1563

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77714-003SUNSCREEN AND INSECT REPELLENT BULL FROG (SPF 50) AEROSOL, SPRAY [BULLFROG BRANDS, LLC]3Current NDC, Legacy NDC, 1 package rows20250112_d5fb3632-24da-2c7a-e053-2a95a90a5081.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
77714-00377714-003-15

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.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sunscreen and insect repellent Bull frogSPF 50Bullfrog Brands, LLCd5fb3632-24da-2c7a-e053-2a95a90a50812025-01-09WarningsExact identifier
ndc (package): 77714-003-15
ndc (product): 77714-003
ndc11 (package): 77714000315
spl id: 2b47aa83-f98f-fa64-e063-6294a90ad217
spl set id: d5fb3632-24da-2c7a-e053-2a95a90a5081

Reported adverse events (FAERS/openFDA)#

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