Home FDA labels 2e02fc7c-4404-195c-e063-6294a90aa9ce Fre Glow Me Lightweight Tinted Moisturizer Light Medium 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 Fre Glow Me Lightweight Tinted Moisturizer Light Medium
Generic name ZINC OXIDE
Manufacturer Peer Pharm Ltd.
Product type HUMAN OTC DRUG
SPL set ID 6815f8d6-0d78-4d4d-8d8c-6a1153a5f61a
SPL ID 2e02fc7c-4404-195c-e063-6294a90aa9ce
Version 3
Effective date 2025-02-13
Source export date 2026-08-08
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-08-08/8e6fb5103b1ab4ab5de5645b4a27f29a2c2739cd9369b81b7befcfa3734d8ef4/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 b39f3b00ad50d2e1b32aaf429248c6081e8799b35bce715b4fccb8cfa1ac4546
Import run 20260810T161303Z
Imported at 2026-08-10 16:45:22 Harmonized routes table Harmonized routes TOPICAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 10 matching rows.
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. Stop use and ask a doctor if rash occurs Keep out of reach of children. If swallowed, call a Poison Control Center or get medical help right away.