Coppertone® Sport Continuous Spray SPF 50

Manufacturer
Bayer HealthCare LLC.
Effective date
2019-08-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:03:58

Label at a glance#

ProductCoppertone Sport
Active ingredientOCTISALATE, OCTOCRYLENE, AVOBENZONE, OXYBENZONE
Label structure14 sections

Indications and uses

• helps prevent sunburn • if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

apply liberally 15 minutes before sun exposure do not spray directly on face. Spray into hands and apply to face. use in well-ventilated areas reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regulatrly use a sunscreen with a Broad ...

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Avobenzone 3%, Octisalate 4.5%, Octocrylene 9%, Oxybenzone 6%

Purpose

OTC - PURPOSE SECTION

Purpose

Sunscreen

Uses

INDICATIONS & USAGE SECTION

• helps prevent sunburn

• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS AND PRECAUTIONS SECTION

For external use only

Flammable: Do not use near heat, flame, or while smoking

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

• keep out of eyes. Rinse with water to remove.

• do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

Stop use and ask doctor if

OTC - STOP USE SECTION

Stop use and ask doctro if rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • do not spray directly on face. Spray into hands and apply to face.
  • use in well-ventilated areas
  • reapply:
  • after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regulatrly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 a.m. - 2 p.m.
  • wear long-sleeve shirts, pants, hats, and sunglasses
  • children under 6 months: Ask a doctor

Other information

OTHER SAFETY INFORMATION

  • protect this product from excessive heat and direct sun
  • avoid long-term storage above 40°C (104°F)
  • may stain or damage some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

SD alcohol 40-B (75.5% v/v), neopentyl glycol diheptanoate, polyester-27, dimethicone, tocopherol (vtimain E), fragrance

Questions?

OTC - QUESTIONS SECTION

1-866-288-3330

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

frontfront

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11523-741011523-7410-1, 11523-7410-2, 11523-7410-3, 11523-7410-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
8f615492-d88e-4a6a-e053-2a95a90aa991553a4f90-6be9-73c1-e054-00144ff8d46c2019-08-05WarningsExact identifier
spl id: 8f615492-d88e-4a6a-e053-2a95a90aa991
spl set id: 553a4f90-6be9-73c1-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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