Dr. Perrys Day Thyme SPF 20 Broad Spectrum 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
Dr. Perrys Day Thyme SPF 20 Broad Spectrum Sunscreen
Generic name
ZINC OXIDE
Manufacturer
Englewood Lab, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
273d8e30-a6bc-4b26-919c-9332fd5197fa
SPL ID
0c5b5d59-a2e3-2550-e063-6394a90aa2bd
Version
8
Effective date
2023-12-12
Source export date
2026-10-30
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:25:40
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

​Warnings ​For external use only. Do not use on damaged or broken skin or mucous membranes or during pregnancy. When using this product keep out of eyes; if product contact eyes, rinse well with water. Stop use and ask a doctor if rash or irritation develops. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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