General Protection

Manufacturer
Cross-Brands Manufacturing LLC
Effective date
2017-02-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:48:56

Label at a glance#

ProductGeneral Protection
Active ingredientHOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE
Label structure1 sections

Label contents#

Full prescribing information#

Sea & Ski SPF 50 Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPF 50 TubeSPF 50 Tube

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130817013020136GTIN-13: 0817013020136
EAN-13: 0817013020136
GTIN-12: 817013020136
UPC-A: 817013020136
GTIN storage (14 digits): 00817013020136
Cross Tube SPF 50.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71153-2013-12020-01-31C16284748780-19d75b9d0-d963-f424-e053-dadaa90a57ceSea & Ski SPF 50 Tube

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71153-2013-1General Protection44 mL in 1 TUBELOTION441

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71153-2013GENERAL PROTECTION (AVOBENZONE,HOMOSALATE,OCTINOXATE,OCTISALATE,OCTOCRYLENE) LOTION [CROSS-BRANDS MANUFACTURING LLC]1Legacy NDC, 1 package rows20170226_49738e31-67ec-0aba-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71153-201371153-2013-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
49738e31-67ed-0aba-e054-00144ff8d46c49738e31-67ec-0aba-e054-00144ff8d46c2017-02-26Exact identifier
spl id: 49738e31-67ed-0aba-e054-00144ff8d46c
spl set id: 49738e31-67ec-0aba-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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