FDA.reportPublic FDA data

Meijer 503.002/503AB Complete Beauty Lotion SPF-15 - Sensitive Skin

Manufacturer
Meijer | Consumer Product Partners, LLC
Effective date
2024-08-21
Label type
HUMAN OTC DRUG LABEL
Version
15
Source
legacy-cache
Hydrated at
2026-08-01 20:56:09

Label at a glance#

ProductComplete Beauty
Active ingredientOCTINOXATE, ZINC OXIDE
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 reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially fr...

Label contents#

Full prescribing information#

Claims

SPL UNCLASSIFIED SECTION

  • LIGHT, NON-GREASY FORMULA
  • DERMATOLOGIST
  • WON'T CLOG PORES
  • FRAGRANCE FREE

When used as directed, Meijer Beauty Lotion helps provide your skin with broad spectrum protecton against premature skin damage from both UVA and UVB rays to help your skin stay younger looking.

ALL DAY MOISTURIZER- This formula with antoxidant vitamin E plus aloe helps promote and maintain healthy-looking skin

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 6.0%

Zinc oxide 3.0%

Purpose

OTC - PURPOSE SECTION

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 SECTION

For external use only

Do Not Use

OTC - DO NOT USE SECTION

on damaged or broken skin

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 at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating
  • 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 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, glycerin, isohexadecane, sodium acrylate/sodium acryloyldimethyl taurate copolymer, polysorbate 80, laureth-7, PEG/PPG-20/20 dimethicone, steareth-21, stearyl alcohol, Gossypium herbaceum (cotton) seed oil, behenyl alcohol, tocopheryl acetate, cetyl alcohol, steareth-2, disodium EDTA, Aloe barbadensis leaf extract, oleth-3 phosphate, benzyl alcohol, chlorphenesin

Disclaimer

SPL UNCLASSIFIED SECTION

May stain or damage some fabrics or surfces

*This product is not manufactured or distributed by Procter & Gamble, distributor of Olay Complete all Day Moisture  Lotion SPF 15

Adverse Reactions

ADVERSE REACTIONS SECTION

Questions-1-888-5943-0593

DIST. BY MEIJER DISTRIBUTION, INC.

GRAND RAPIDS,MI49544

www.meijer.com

principl display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to

Olay Complete

All Day Moisture

Sensitive Skin

meijer

beauty

lotion

WITH SUNSCREEN

Broad Spectrum SPF 15

FOR SENSITIVE SKIN

UVA/UVB Protection

Antioxidant Vitamin E Plus Aloe

Fragrance Free

6 FL OZ (177 mL)

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41250-95541250-955-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ISOHEXADECANE918X1OUF1EIACT
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)1DXE3F3OZXIACT
POLYSORBATE 806OZP39ZG8HIACT
LAURETH-7Z95S6G8201IACT
PEG/PPG-20/20 DIMETHICONEBA94B7CK8KIACT
STEARETH-2153J3F32P58IACT
STEARYL ALCOHOL2KR89I4H1YIACT
LEVANT COTTONSEED OILN5CFT140R8IACT
DOCOSANOL9G1OE216XYIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CETYL ALCOHOL936JST6JCNIACT
STEARETH-2V56DFE46J5IACT
EDETATE DISODIUM7FLD91C86KIACT
ALOE VERA LEAFZY81Z83H0XIACT
OLETH-3 PHOSPHATE8Q0Z18J1VLIACT
BENZYL ALCOHOLLKG8494WBHIACT
CHLORPHENESINI670DAL4SZIACT
OCTINOXATE4Y5P7MUD51ACTIB
ZINC OXIDESOI2LOH54ZACTIB

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
25279b0f-1d6d-18aa-e063-6294a90a6d6275471e8e-2dae-44a0-a35a-5563f43b56832024-10-23Warnings, Adverse reactionsExact identifier
spl set id: 75471e8e-2dae-44a0-a35a-5563f43b5683

Reported adverse events (FAERS/openFDA)#

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