Coppertone Ultra Guard Spray SPF 50 (Aerosol)

Manufacturer
Bayer HealthCare LLC.
Effective date
2019-08-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:04:44

Label at a glance#

ProductCoppertone Ultra Guard SPF 50
Active ingredientAVOBENZONE, OXYBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure14 sections

Indications and uses

Uses ■ helps prevent sunburn

Dosage and administration

Directions ■ shake well before use ■ apply liberally 15 minutes before sun exposure and rub into skin ■ 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 ...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

(To Deliver) Avobenzone 3%, Homosalate 10%, Octisalate 4.5%,

Octocrylene 9%, Oxybenzone 2%

Purpose

OTC - PURPOSE SECTION

Purpose

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Uses

■ helps prevent sunburn

Warnings

WARNINGS SECTION

Warnings
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

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

■ use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

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

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor 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 Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

■ shake well before use

■ apply liberally 15 minutes before sun exposure and rub into skin

■ 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, regularly 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

Other information

■ protect this product from excessive heat and direct sun

■ store between 20˚ to 25˚C (68˚ to 77˚F)

■ may stain or damage some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients SD alcohol 40-B (50.3% v/v), isobutane, isohexadecane, isododecane, dimethicone, VA/butyl maleate/isobornyl acrylate copolymer, C13-15 alkane, tocopherol (vitamin E), fragrance

Questions

OTC - QUESTIONS SECTION

Questions? 1-866-288-3330

Package display label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Coppertone®

Sunscreen Spray

ULTRA

GUARD®

INTENSE

DEFENSE 50

Protests Against

Damaging UVA/UVB Rays

Water Resistant (80 Minutes)

Broad Spectrum SPF 50

Product labelProduct label

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11523-742611523-7426-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
8fa0ac5f-bcc9-484d-e053-2a95a90ada8b5e32fcff-d53e-98ad-e053-2991aa0a96f72019-08-08WarningsExact identifier
spl id: 8fa0ac5f-bcc9-484d-e053-2a95a90ada8b
spl set id: 5e32fcff-d53e-98ad-e053-2991aa0a96f7

Reported adverse events (FAERS/openFDA)#

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