Nudestix Daily Mineral Veil SPF 30 Tint - Warm

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
Nudestix Daily Mineral Veil SPF 30 Tint - Warm
Generic name
ZINC OXIDE 15%
Manufacturer
Bentley Laboratories, LLC
Product type
HUMAN OTC DRUG
SPL set ID
d5fd3fea-5dcf-42ef-927a-3b4a3e1ccff8
SPL ID
da8723c1-1d02-47a9-82ad-0ea4527c721c
Version
3
Effective date
2023-12-19
Source export date
2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:38:51
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. / si une éruption cutanée se développe.

Reported adverse events (FAERS/openFDA)#

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