MOISTURIZING SUNSCREEN SPF15

Manufacturer
Shine & Pretty (USA), Corp.
Effective date
2011-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:30:20

Label at a glance#

ProductMOISTURIZING SUNSCREEN SPF15
Active ingredientOXYBENZONE, OCTINOXATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

For Sun protection: Apply on surfaces of skin, on face, arm and hand. SPF-15 provides the face and body skin with effective protection against harmful UVA and UVB rays. Use daily over moisture cream to help prevent premature aging and wrinkling due to prolonged exposure to the sun, reapply after swimming or excessive exercise.

INDICATIONS & USAGE SECTION

Smear Lightly.

WARNINGS SECTION

Warning: For external use only, not to be swallowed. Avoid contact with eye. Discontinue if signs of irritation or rash appear.

DOSAGE & ADMINISTRATION SECTION

To Apply lightly.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: SORBITAN SESQUIOLEATE, POLYSORBATE 60, CARBOMER 934, VITAMIN E ACETATE, STEARIC ACID, PROPYLENE GLYCOL, VITAMIN A PALMITATE, PROPYLPARABEN, Water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of the reach of children. Use on children under six months of age only with the advice of a physician.

OTC - ACTIVE INGREDIENT SECTION

OXYBENZONE and OCTINOXATE.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MM1labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59663-001-012019-11-13C16284748780-197449f38-d58c-f6ea-e053-dbdaa90aa7033a0b9ac4-12c0-4ef9-a4e1-56c2ea21dc49

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59663-001-01MOISTURIZING SUNSCREEN SPF15100 mL in 1 BOTTLELOTION1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59663-001MOISTURIZING SUNSCREEN SPF15 (OXYBENZONE) LOTION [SHINE & PRETTY (USA), CORP.]1Legacy NDC, 1 package rows20111216_3a0b9ac4-12c0-4ef9-a4e1-56c2ea21dc49.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OXYBENZONEACTIVE MOIETY95OOS7VE0Y1

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59663-00159663-001-01

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
887b89ab-92bf-4bfa-b6b3-73539f94255c3a0b9ac4-12c0-4ef9-a4e1-56c2ea21dc492011-06-02WarningsExact identifier
spl id: 887b89ab-92bf-4bfa-b6b3-73539f94255c
spl set id: 3a0b9ac4-12c0-4ef9-a4e1-56c2ea21dc49

Reported adverse events (FAERS/openFDA)#

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