PHOTO-AGE SUNSCREEN

Manufacturer
ADVANCED AESTHETICS
Effective date
2023-01-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:53:14

Label at a glance#

ProductPHOTO-AGE SUNSCREEN SPF 30
Active ingredientOCTINOXATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, OXYBENZONE
Label structure8 sections

Indications and uses

HELPS PREVENT SUNBURN. HIGHER SPF PROVIDES MORE SUNBURN PROTECTION.

Dosage and administration

APPLY SUNSCREEN TO ALL EXPOSED AREAS 30 MINUTES BEFORE GOING OUTDOORS. MASSAGE THOROUGHLY INTO SKIN AND ALLOW TO ABSORB. REAPPLY EVERY TWO HOURS TO ENSURE MAXIMUM PROTECTION - MORE FREQUENTLY WHEN SWIMMING OR ACTIVE.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

OCTINOXATE (ETHYLHEXYL METHOXYCINNAMATE)  7.5%

TITANIUM DIOXIDE 6%

OCTISALATE (ETHYLHEXYL SALICYLATE)  5%

OCTOCRYLENE  1.5%

OXYBENZONE (BENZOPHENONE-3)  1%

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USES

INDICATIONS & USAGE SECTION

HELPS PREVENT SUNBURN. HIGHER SPF PROVIDES MORE SUNBURN PROTECTION.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE.

STOP USE AND ASK A DOCTOR IF RASH OCCURS.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY SUNSCREEN TO ALL EXPOSED AREAS 30 MINUTES BEFORE GOING OUTDOORS. MASSAGE THOROUGHLY INTO SKIN AND ALLOW TO ABSORB. REAPPLY EVERY TWO HOURS TO ENSURE MAXIMUM PROTECTION - MORE FREQUENTLY WHEN SWIMMING OR ACTIVE.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

AQUA (WATER), CYCLOPENTASILOXANE, GLYCERIN, CETYL ALCOHOL, C12-15 ALKYL BENZOATE, POTASSIUM CETYL PHOSPHATE, STEARIC ACID, DIMETHICONE, CETYL DIMETHICONE, CAPRYLYL METHICONE, GLYCERYL STEARATE, PEG-100 STEARATE, VP/EICOSENE COPOLYMER, ALUMINA, ALUMINUM STARCH OCTENYLSUCCINATE, HYDROGENATED VEGETABLE OIL, TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE, PEG-40 HYDROGENATED CASTOR OIL, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, BORON NITRIDE, CAPRYLYL GLYCOL, LECITHIN, PHENOXYETHANOL, SQUALANE, CARBOMER, POLYHYDROXYSTEARIC ACID, CHLORPHENESIN, CITRUS AURANTIUM DULCIS (ORANGE) PEEL OIL, CARRAGEENAN, HEXYLENE GLYCOL, SODIUM HYDROXIDE, CARICA PAPAYA (PAPAYA) FRUIT EXTRACT, TOCOPHERYL ACETATE, DISODIUM EDTA, VITIS VINIFERA (GRAPE) SEED EXTRACT, SODIUM HYALURONATE, CAMELLIA SINENSIS LEAF EXTRACT, RETINYL PALMITATE, ASCORBYL PALMITATE.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_GlyMed Photo-Age Sunscreen SPF-30_2oz01b UC_GlyMed Photo-Age Sunscreen SPF-30_2oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62551-213-522025-01-30C16284748780-12cef2736-6996-d83d-e063-dadaa90ab31fADV AESTHETICS - GLYMEDPLUS MASTER AESTHETICS ELITE PHOTO-AGE SUNSCREEN SPF 30+ (62551-213)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62551-213-12PHOTO-AGE SUNSCREENSPF 3056 mL in 1 TUBEGEL563
62551-213-52PHOTO-AGE SUNSCREENSPF 301 in 1 BOXGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62551-213PHOTO-AGE SUNSCREEN SPF 30 (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) GEL [ADVANCED AESTHETICS]3Legacy NDC, 2 package rows20230113_8ebaf67f-33f1-4f32-9d8f-7e51bec35e75.zip

Products#

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

DailyMed product names page 1 of 2 · 46 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62551-21362551-213-12, 62551-213-52

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 44 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
f219c41d-a661-2360-e053-2995a90a8e568ebaf67f-33f1-4f32-9d8f-7e51bec35e752023-01-12WarningsExact identifier
spl id: f219c41d-a661-2360-e053-2995a90a8e56
spl set id: 8ebaf67f-33f1-4f32-9d8f-7e51bec35e75

Reported adverse events (FAERS/openFDA)#

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