Sunscreen

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
Sunscreen
Generic name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Manufacturer
Amazon.com Services LLC
Product type
HUMAN OTC DRUG
SPL set ID
d4b4ebac-c6c2-474b-afc6-b80b8431e90f
SPL ID
4c212fda-1319-8ed8-e063-6294a90ab8fd
Version
18
Effective date
2026-03-03
Source export date
2026-10-27
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:49:11
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

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTION May stain or damage some fabrics or surfaces DIST. BY Amazon.com Services, LLC Seattle, WA 98109 1-877-485-0385 ©2019 Amazon. com, Inc or its affiliates. All rights reserved.

Reported adverse events (FAERS/openFDA)#

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