NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Sunkissed Glow

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
NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Sunkissed Glow
Generic name
ZINC OXIDE SUNSCREEN
Manufacturer
Bentley Laboratories, LLC
Product type
HUMAN OTC DRUG
SPL set ID
bf1a237b-b27e-4c55-8ded-e348240a5b9a
SPL ID
7a12c26c-723b-40cb-9960-8e7137c86d13
Version
1
Effective date
2026-02-06
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:32:07
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 / Mises en garde For external use only / Pour usage externe seulement When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. / Lorsque vous utilisez ce produit éviter tout contact avec les yeux. Le cas échéant, bien rincer avec de l’eau. Stop use and consult a health care practitioner if rash occurs. / Arrêter l’utilisation et consultez un professionnel de la santé en cas d’éruption cutanée

Reported adverse events (FAERS/openFDA)#

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