FDA.reportPublic FDA data

ILLUMINATING DAILY MOISTURIZER

Manufacturer
CVS PHARMACY INC
Effective date
2010-08-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:26

Label at a glance#

ProductILLUMINATING DAILY MOISTURIZER SPF 30
Active ingredientHOMOSALATE, OCTISALATE, AVOBENZONE, OXYBENZONE, OCTOCRYLENE
Label structure5 sections

Indications and uses

USES: HELPS PREVENT SUNBURN. HIGHER SPF GIVES MORE SUNBURN PROTECTION. DIRECTIONS: APPLY EVENLY BEFORE SUN EXPOSURE. AFTER CLEANSING, SMOOTH OVER FACE AND NECK DAILY.

Dosage and administration

USES: HELPS PREVENT SUNBURN. HIGHER SPF GIVES MORE SUNBURN PROTECTION. DIRECTIONS: APPLY EVENLY BEFORE SUN EXPOSURE. AFTER CLEANSING, SMOOTH OVER FACE AND NECK DAILY.

Storage and handling

STORE AT ROOM TEMPERATURE.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

  • AVOBENZONE 3% (SUNSCREEN)
  • HOMOSALATE 12% (SUNSCREEN)
  • OCTISALATE 5% (SUNSCREEN)
  • OCTOCRYLENE 1.7% (SUNSCREEN)
  • OXYBENZONE 3% (SUNSCREEN)

USES AND DIRECTIONS

OTC - PURPOSE SECTION

  • USES: HELPS PREVENT SUNBURN. HIGHER SPF GIVES MORE SUNBURN PROTECTION.
  • DIRECTIONS: APPLY EVENLY BEFORE SUN EXPOSURE. AFTER CLEANSING, SMOOTH OVER FACE AND NECK DAILY.

WARNINGS

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER.

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

RASH OR REDNESS DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

STORE AT ROOM TEMPERATURE.

PACKAGE LABELS/ Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

  • Front and Back Labels: cvs2.5.jpg2.5OZ FRONT AND BACK LABELS2.5OZ FRONT AND BACK LABELS
  • Carton: cvs1.jpgCARTON 1CARTON 1
  • Carton: cvs2.jpgCARTON 2CARTON 2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59779-326-032020-01-31C16284748780-19d75b9d0-d3e4-f424-e053-dadaa90a57ceDRUG FACTS BOX

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59779-326-00ILLUMINATING DAILY MOISTURIZERSPF 3074 mL in 1 BOTTLE, PUMPLOTION741
59779-326-03ILLUMINATING DAILY MOISTURIZERSPF 301 in 1 CARTONLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59779-326ILLUMINATING DAILY MOISTURIZER SPF 30 (HOMOSALATE) LOTION [CVS PHARMACY INC]1Legacy NDC, 2 package rows20100805_652b6f1c-c4d9-4c01-9b68-9c0403d01c3c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
HOMOSALATEACTIVE INGREDIENTV06SV4M95S1
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
OCTOCRYLENEACTIVE INGREDIENT5A68WGF6WM1
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
HOMOSALATEACTIVE MOIETYV06SV4M95S1
OCTISALATEACTIVE MOIETY4X49Y0596W1
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM1
OXYBENZONEACTIVE MOIETY95OOS7VE0Y1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59779-32659779-326-00, 59779-326-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
OXYBENZONE95OOS7VE0YACTIB
OCTOCRYLENE5A68WGF6WMACTIB

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
81bfb623-57f7-4a15-877f-5b2184a2e871652b6f1c-c4d9-4c01-9b68-9c0403d01c3c2010-08-04WarningsExact identifier
spl id: 81bfb623-57f7-4a15-877f-5b2184a2e871
spl set id: 652b6f1c-c4d9-4c01-9b68-9c0403d01c3c

Reported adverse events (FAERS/openFDA)#

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