FDA.reportPublic FDA data

SEA STAR SPARKLE SPF 50 Glitter Sunscreen Coco Lime

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
SEA STAR SPARKLE SPF 50 Glitter Sunscreen Coco Lime
Generic name
HOMOSALATE, OCTOCRYLENE, OCTISALATE, ZINC OXIDE
Manufacturer
MJ Products Association, LLC
Product type
HUMAN OTC DRUG
SPL set ID
533b6106-7f6f-49b9-9670-e2050bfcb932
SPL ID
09749db1-19bf-799e-e063-6294a90a47eb
Version
3
Effective date
2023-11-05
Source export date
2026-08-17
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-17/f2a007a22a89560a66943d28521709913d039c2d0cd7e278faf1082cd194c72c/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 07:18:48
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and consult physician if irritation or rash develops. Keep out of reach of children. If product is swallowed, get medical attention or contact poison control center immediately.