Sea & Ski GP Sunscreen Lotion

Manufacturer
Cross-Brands Manufacturing, LLC
Effective date
2016-12-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:48:14

Label at a glance#

Productgp sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71153-2000-12020-01-31C16284748780-19d75b9cf-ed62-f424-e053-dadaa90a57ceSea & Ski GP Sunscreen Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71153-2000-1gp sunscreen237 mL in 1 BOTTLELOTION2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71153-2000GP SUNSCREEN (AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE) LOTION [CROSS-BRANDS MANUFACTURING, LLC]1Legacy NDC, 1 package rows20161223_444a04b9-c142-2c14-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71153-200071153-2000-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
444a04b9-c143-2c14-e054-00144ff8d46c444a04b9-c142-2c14-e054-00144ff8d46c2016-12-22Exact identifier
spl id: 444a04b9-c143-2c14-e054-00144ff8d46c
spl set id: 444a04b9-c142-2c14-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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