FDA.reportPublic FDA data

Seavenger ocean kiss sunscreen SPF 50

Manufacturer
SHOP 709 Corp
Effective date
2023-12-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:05:43

Label at a glance#

ProductSeavenger ocean kiss sunscreen SPF 50
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure9 sections

Indications and uses

Helps prevent sunburns  Anti-Jellyfish Sting Formula Coral Reef Safe (Octinoxate & Oxybenzone Free)

Dosage and administration

Apply liberally to skin 15 minutes before sun exposure  Reapply: at least every 2 hours, immediately after towel drying or after 80 minutes of swimming or sweating Children under 6 months: ask a doctor.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide (Non-Nano) 11.9%
Zinc Oxide (Non-Nano) 1%

Purpose

OTC - PURPOSE SECTION

Sunscreen for all skin types

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburns 
  • Anti-Jellyfish Sting Formula
  • Coral Reef Safe (Octinoxate & Oxybenzone Free)

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally to skin 15 minutes before sun exposure 
  • Reapply: at least every 2 hours, immediately after towel drying or after 80 minutes of swimming or sweating
  • Children under 6 months: ask a doctor.

Warnings

WARNINGS SECTION

  • For External Use Only

Do not use

OTC - DO NOT USE SECTION

  • on damaged or broken skin
  • Keep out of eyes
  • Rinse with water to remove 
  • May cause irritation 

Stop use and ask a doctor 

OTC - STOP USE SECTION

  • if a rash occurs

Keep out of children's reach 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, seek medical help or contact Poison
  • Control Center immediately

Information

SPL UNCLASSIFIED SECTION

This product should not be used as guarateed protection in jellyfish-infested waters, sting(s) can occur. In case of a sting(s), seek medical attention.

Caution

SPL UNCLASSIFIED SECTION

  • Store container in a dry environment:avoid excessive heat or direct sunlight 
  • If discomfort occurs, discontinue use and consult a dermatologist

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Caprylyl Methicone, Caprylic/Capric Triglyceride, Butylene Glycol, Ethylhexyl Stearate, Lauryl PEG-10 Tris (Trimethylsiloxy) Silylethyl Dimethicone, Glycerin, Cyclopentasiloxane, C12-15 Alkyl Benzoate, Talc, Isononyl Isononanoate, PEG-10 Dimethicone, Polyhydroxystearic Acid, Magnesium sulfate, Sodium chloride, Alumina, Phenoxyethanol, Chlorphenesin, Phenyl Trimethicone, Stearic Acid, Dimethiconol, Dimethicone, 5 Ethylhexylglycerin, Dimethiconol Crosspolymer, Lauroyl Lysine, Squalane, Maltodextrin, Tocopheryl Acetate, Maltodextrin, Tocopheryl Acetate, Sodium Benzoate, Laminaria Ochroleuca Extract, Marrubium Vulare Extract, Caesalpinia Spinosa Fruit Extract, Helianthus Annuus Sprout Extract

Questions?

OTC - QUESTIONS SECTION

Contact: care@seavenger.com

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82588-001-012025-07-29C16284748780-13b156c62-2509-fb37-e063-e6dba90a4e07Seavenger ocean kiss sunscreen SPF 50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82588-001-01Seavenger ocean kiss sunscreen SPF 50118 mL in 1 TUBECREAM1183
82588-001-01Seavenger ocean kiss sunscreen SPF 501 in 1 CARTONCREAM13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82588-001SEAVENGER OCEAN KISS SUNSCREEN SPF 50 (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [SHOP 709 CORP]3Legacy NDC, 2 package rows20231227_dacfe6ba-103e-99e9-e053-2995a90a25bb.zip

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82588-00182588-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
GLYCERINPDC6A3C0OXIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
TALC7SEV7J4R1UIACT
ISONONYL ISONONANOATES4V5BS6GCXIACT
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABIACT
SODIUM CHLORIDE451W47IQ8XIACT
ALUMINUM OXIDELMI26O6933IACT
PHENOXYETHANOLHIE492ZZ3TIACT
CHLORPHENESINI670DAL4SZIACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
STEARIC ACID4ELV7Z65APIACT
DIMETHICONE92RU3N3Y1OIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
LAUROYL LYSINE113171Q70BIACT
SQUALANEGW89575KF9IACT
MALTODEXTRIN7CVR7L4A2DIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM BENZOATEOJ245FE5EUIACT
LAMINARIA OCHROLEUCA4R2124HE76IACT
HELIANTHUS ANNUUS SPROUT4P26HG1S5WIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIM

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
0d6d5a93-c97f-3c03-e063-6394a90a9f4bdacfe6ba-103e-99e9-e053-2995a90a25bb2023-12-26WarningsExact identifier
spl id: 0d6d5a93-c97f-3c03-e063-6394a90a9f4b
spl set id: dacfe6ba-103e-99e9-e053-2995a90a25bb

Reported adverse events (FAERS/openFDA)#

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