Venture Performance Sun Protection Mineral Sunscreen SPF 50

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
Venture Performance Sun Protection Mineral Sunscreen SPF 50
Generic name
ZINC OXIDE
Manufacturer
Venture Performance Inc
Product type
HUMAN OTC DRUG
SPL set ID
630fc5c2-a315-4e26-9bd9-5f8533d75908
SPL ID
44e43ee5-cd83-bd65-e063-6294a90a49bb
Version
1
Effective date
2025-12-01
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:26:28
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 Do not use ● on damaged or broken skin. When using this product ● keep out of eyes, rinse with water to remove. ● Do not puncture of incinerate. Contents under pressure. Do not store at temperatures above 120°F. Stop use and ask a doctor if ● rash or irritation develops and lasts. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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