Coppertone UltraGuard Aerosol Spray SPF 50, UI1614352

Manufacturer
Bayer HealthCare LLC.
Effective date
2019-12-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:50:28

Label at a glance#

ProductCoppertone Ultra Guard SPF 50
Active ingredientOCTISALATE, OCTOCRYLENE, AVOBENZONE, HOMOSALATE
Label structure10 sections

Indications and uses

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

Directions ■ 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, regularly us...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 5%

OTC - PURPOSE SECTION

Purpose

Sunscreen

Uses

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings

For external use only

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

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.

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

OTC - STOP USE 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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

■ 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, 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

■ avoid long-term storage above 40˚C (104˚F)

■ may stain or damage some fabrics or surfaces

INACTIVE INGREDIENT SECTION

Inactive ingredients SD alcohol 40-B (73.8% v/v), neopentyl glycol diheptanoate, polyester-27, acrylates/octylacrylamide copolymer, dimethicone, fragrance, ascorbyl palmitate

OTC - QUESTIONS SECTION

Questions? 1-866-288-3330

Can 156 grams

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LIMITED EDITION

Coppertone®

Sunscreen Spray

50

Protects against damaging

UVA/UVB rays

Water Resistant (80 Minutes)

Broad Spectrum SPF 50

NET WT 5.5 OZ. (156 g)

Can 5.5 oz.Can 5.5 oz.

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11523-744611523-7446-1, 11523-7446-2, 11523-7446-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
99fe9eef-55aa-d33b-e053-2995a90a3c858f0f985b-4ac0-c0a0-e053-2a95a90ae0972019-12-18WarningsExact identifier
spl id: 99fe9eef-55aa-d33b-e053-2995a90a3c85
spl set id: 8f0f985b-4ac0-c0a0-e053-2a95a90ae097

Reported adverse events (FAERS/openFDA)#

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