FDA.reportPublic FDA data

Sea & Ski SPF 15 Spray

Manufacturer
Cross-Brands Manufacturing, LLC
Effective date
2019-01-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:58:06

Label at a glance#

ProductSPF 15
Active ingredientHOMOSALATE, AVOBENZONE, OCTISALATE
Label structure1 sections

Label contents#

Full prescribing information#

Sea & Ski SPF 15 Continuous Spray

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sea & Ski SPF 15 CSpraySea & Ski SPF 15 CSpray

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71153-2014-12020-09-27C16284748780-1ab0e2407-2e70-f274-e053-dbdaa90a6471Sea & Ski SPF 15 Spray
71153-2014-12020-09-25C16284748780-1ab0e2407-2e70-f274-e053-dbdaa90a6471Sea & Ski SPF 15 Spray
71153-2014-12020-07-22C16284748780-1ab0e2407-2e70-f274-e053-dbdaa90a6471Sea & Ski SPF 15 Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71153-2014-1SPF 15170 mL in 1 CANAEROSOL, SPRAY1702

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71153-2014SPF 15 (AVOBENZONE, OCTISALATE, HOMOSALATE) AEROSOL, SPRAY [CROSS-BRANDS MANUFACTURING, LLC]2Legacy NDC, 1 package rows20190109_51b42037-a0b2-5646-e054-00144ff8d46c.zip

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
71153-201471153-2014-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
ALOE VERA LEAFZY81Z83H0XIACT

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
7ef772ff-3e61-5b1c-e053-2a91aa0a35e751b42037-a0b2-5646-e054-00144ff8d46c2019-01-08Exact identifier
spl id: 7ef772ff-3e61-5b1c-e053-2a91aa0a35e7
spl set id: 51b42037-a0b2-5646-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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