FDA.reportPublic FDA data

COCO EVE BODY SUNSCREEN SPF50 plus

Manufacturer
Supernova USA Inc. | Baxter Laboratories Pty. Ltd.
Effective date
2022-11-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:52:55

Label at a glance#

ProductCOCO EVE BODY SUNSCREEN SPF50 plus
Active ingredientHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Label structure8 sections

Storage and handling

Other information Protect the product from excessive heat and direct sun Questions? Contact (626) 616-5811

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Homosalate 10%
Octocrylene 8%
Octisalate 5%
Avobenzone 3%		Purpose
Sunscreen
Sunscreen
Sunscreen
Sunscreen

INDICATIONS & USAGE SECTION

Uses

  • Helps prevent sunburn.
  • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS SECTION

Warnings

For external use only.

Store below 30°C / 86°F and avoid direct sunlight.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. When using this product keep out of eyes. Rinse with water to remove.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply an even layer on skin 20 minutes before sun exposure.
  • Reapply frequently especially after swimming, swaeting, or towelling.
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad-spectrum SPF of 15 or higher and other sun protection measures including:
    • limit time in the sun, especially from 10 a.m. - 2. p.m.
    • Wear a long-sleeve shirts, pants, hats, and sunglasses.
  • Children under 6 months: ask a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water (Aqua), Beeswax, Aloe Barbadensis Leaf Juice, Isopropyl Palmitate, Cetearyl Alcohol, Cyclopentasiloxane, Cyclohexasiloxane, Ceteareth-20, Hydroxyacetophenone, Carbomer, Benzyl Alocohol, Phenoxyethanol, Sodium Stearoyl Glutamate, Triethanolamine, Tocopheryl Acetate, Cocos Nucifera (Coconut) Oil, Citric Acid.

STORAGE AND HANDLING SECTION

Other information

Protect the product from excessive heat and direct sun

Questions? Contact (626) 616-5811

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COCO & EVE

BODY SUNSCREEN

SPF 50+

LOTION SOLAIRE
CORPORELLE SPF 50+

UVA + UVB

Broad Spectrum SPF 50+

80 Minutes Water Resistant

Lightweight

Net 200 mL / 6.76 fl. oz. US

FIGURE1FIGURE1

COCO & EVE

BODY SUNSCREEN

SPF 50+

LOTION SOLAIRE
CORPORELLE SPF 50+

UVA + UVB

Broad Spectrum SPF 50+

80 Minutes Water Resistant

Lightweight

Net 200 mL / 6.76 fl. oz. US

FIGURE2FIGURE2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82931-003-202025-01-30C16284748780-12cef2736-6543-d83d-e063-dadaa90ab31fCOCO & EVE BODY SUNSCREEN SPF 50+

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82931-003-20COCO EVE BODY SUNSCREEN SPF50 plus1 in 1 CARTONLOTION12
82931-003-20COCO EVE BODY SUNSCREEN SPF50 plus200 mL in 1 BOTTLE, PLASTICLOTION2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82931-003COCO EVE BODY SUNSCREEN SPF50 PLUS LOTION [SUPERNOVA USA INC.]2Legacy NDC, 2 package rows20230105_119df9dc-3fd7-4005-ab8f-3d018c2bc754.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82931-00382931-003-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
WATER059QF0KO0RIACT
YELLOW WAX2ZA36H0S2VIACT
ALOE VERA LEAFZY81Z83H0XIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CYCLOMETHICONE 50THT5PCI0RIACT
CYCLOMETHICONE 6XHK3U310BAIACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
BENZYL ALCOHOLLKG8494WBHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
COCONUT OILQ9L0O73W7LIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
2ff24811-2e53-4bed-a115-a60461d10781119df9dc-3fd7-4005-ab8f-3d018c2bc7542022-11-16WarningsExact identifier
spl id: 2ff24811-2e53-4bed-a115-a60461d10781
spl set id: 119df9dc-3fd7-4005-ab8f-3d018c2bc754

Reported adverse events (FAERS/openFDA)#

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