FDA.reportPublic FDA data

Kroger D54.000/D54AA Moisturizing Sunscreen Lotion SPF 50

Manufacturer
The Kroger Co. | Nice-Pak Products, LLC
Effective date
2026-02-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
monthly-update
Hydrated at
2026-06-03 17:58:08

Label at a glance#

ProductMoisturizing Sunscreen SPF 50
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE
Label structure15 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protections 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 apply to all skin exposed to the sun 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 protecti...

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 12%

Octisalate 5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • if used as directed with other sun protections measures (see Directions), decreases the risk 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
  • apply to all skin exposed to the sun
  • 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-sleeved shirts, pants, hats and sunglasses
  • children under 6 months of age: Ask a doctor

Other Information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, diethylhexyl 2,6-naphthalate, butyloctyl salicylate, styrene/acrylates copolymer, aluminum starch octenylsuccinate, neopentyl glycol diheptanoate, glyceryl stearate, silica, polyester-7, beeswax, acrylates/C10-30 alkyl acrylate crosspolymer, glycerin, potassium hydroxide, chlorphenesin, tocopherol, benzyl alcohol, arachidyl alcohol, fragrance, PEG-100 stearate, behenyl alcohol, arachidyl glucoside, disodium EDTA, amyl cinnamal, sodium ascorbyl phosphate

Questions?

OTC - QUESTIONS SECTION

1-800-632-6900

Disclaimers

SPL UNCLASSIFIED SECTION

May stain or damage some fabrics or surfaces

*COPPERTONE ® IS A REGISTERED TRADEMARK OF BEIERSDORF AG. BEIERSDIRF AG IS NOT AFFILIATED WITH THE KROGER CO. OR THIS PRODUCT.

Adverse Reactions

ADVERSE REACTIONS SECTION

DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202

QUALITY GUARANTEE

800-632-6900

www.kroger.com

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

compare to COPPERTONE ® COMPLETE LOTION SPF 50

*see back panel

Kroger ®

SUNSCREEN lotion

BROAD SPECTRUM SPF 50

UVA/UVB sunscreen

hypoallergenic

water resistant (80 minutes)

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 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59450-95459450-954-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
DIETHYLHEXYL 2,6-NAPHTHALATEI0DQJ7YGXMIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW)5Z4DPO246AIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
POLYESTER-70841698D2FIACT
YELLOW WAX2ZA36H0S2VIACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
CHLORPHENESINI670DAL4SZIACT
TOCOPHEROLR0ZB2556P8IACT
BENZYL ALCOHOLLKG8494WBHIACT
ARACHIDYL ALCOHOL1QR1QRA9BUIACT
PEG-100 STEARATEYD01N1999RIACT
DOCOSANOL9G1OE216XYIACT
ARACHIDYL GLUCOSIDE6JVW35JOOJIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
.ALPHA.-AMYLCINNAMALDEHYDEWC51CA3418IACT
SODIUM ASCORBYL PHOSPHATE836SJG51DRIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB

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
4ffc6f54-2a0e-d732-e063-6394a90a7226e6b5095c-7592-4da8-b112-0bbc1c9873012026-04-21Warnings, Adverse reactionsExact identifier
spl set id: e6b5095c-7592-4da8-b112-0bbc1c987301

Reported adverse events (FAERS/openFDA)#

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