Kroger 711.000/711 rev 1 Ultra Sunscreen Lotion SPF 50

Manufacturer
The Kroger Co | Consumer Product Partners, LLC
Effective date
2024-09-11
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
legacy-cache
Hydrated at
2026-08-01 20:55:07

Label at a glance#

ProductSunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure15 sections

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 ​Sun Protection Measures.  ​Spending time in the sun increases your risk of skin cancer and early skin aging.  To decrease this risk use a  reqularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit t...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 13%

Octisalate 5%

Octocrylene 7%

Oxybenzone 4%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes.  Rinse with water to remove

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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
  • ​Sun Protection Measures. ​Spending time in the sun increases your risk of skin cancer and early skin aging.  To decrease this risk use a  reqularly 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-sleeved shirts, pants, hats and sunglasses
  • children under 6 months of age: Ask a doctor

Other Information

SPL UNCLASSIFIED SECTION

  • Protect the product from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sorbitol, triethanolamine, VP/eicosene copolymer, stearic acid, sorbitan isostearate, aluminum starch octenylsuccinate, benzyl alcohol, dimethicone, tocopheryl, chlorphenesin, polyglyceryl-3 distearate, fragrance, carbomer, disodium EDTA

Questions or comments?

OTC - QUESTIONS SECTION

1-800-632-6900

Adverse Reaction

ADVERSE REACTIONS SECTION

DISTRIBUTED BY THE KROGER CO.
CINCINNATI, OHIO 45202

Disclaimer

SPL UNCLASSIFIED SECTION

COPPERTONE AND COPPERTONE ULTRA GUARD ARE REGISTERED TRADEMARKS OF BAYER, WHIPPANY, NJ 07981.  BAYER IS NOT AFFILIATED WITH THE KROGER CO. OR THIS PRODUCT

May stain or damage some fabrics or surfaces.

QUALITY GUARANTEE

800-632-6900

www.kroger.com

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

compare to COPPERTONE

ULTRA GUARD see back panel

Kroger

SUNSCREEN

LOTION

BROAD SPECTRUM SPF 50

UVA/UVB sunscreen

hypoallergenic

water resistant (80 minutes)

enriched with moisturizers

non-greasy

SPF

50

8 FL OZ (236 mL)

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30142-71130142-711-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
25141503-e979-b6c1-e063-6394a90a03ad470274a8-2387-4564-be2e-962cb5c7978c2024-10-22Warnings, Adverse reactionsExact identifier
spl set id: 470274a8-2387-4564-be2e-962cb5c7978c

Reported adverse events (FAERS/openFDA)#

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