NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Angel 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 - Angel Glow
Generic name
ZINC OXIDE SUNSCREEN
Manufacturer
Bentley Laboratories, LLC
Product type
HUMAN OTC DRUG
SPL set ID
351217c4-8d71-41d9-ab08-c43857c0510c
SPL ID
c763fc26-8db9-4d78-b229-bb6020deb183
Version
1
Effective date
2026-02-04
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:02:35
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.