ULTRALIGHT AGE DEFENSE 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
ULTRALIGHT AGE DEFENSE SPF 50
Generic name
ZINC OXIDE
Manufacturer
Guangzhou Origin Beauty Cosmetics Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
4e36a743-7906-2b7b-e063-6294a90af314
SPL ID
4e36a743-7907-2b7b-e063-6294a90af314
Version
1
Effective date
2026-03-29
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 06:27:16
Harmonized routes table
Harmonized routes
CUTANEOUS

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

For external use only Do not use on damaged or broken skin. When using the product Keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away. Directions Apply liberally 15 minutes before sun exposure Reapply: After 40 minutes of swimming

Reported adverse events (FAERS/openFDA)#

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