warnings
For external use only. on damaged or broken skin. keep out of eyes. Rinse with water to remove. if product is swallowed, get medical help or contact a Poison Control Center right away.
Naturium Dew Glow Tinted Moisturizer SPF50-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
- Brand name
- Naturium Dew Glow Tinted Moisturizer SPF50-medium
- Generic name
- HOMOSALATE, OCTISALATE, AVOBENZONE
- Manufacturer
- PML NYC, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1c3489a6-5b98-2dc2-e063-6294a90a0695
- SPL ID
- 4f782e36-b736-efc7-e063-6394a90adfda
- Version
- 5
- Effective date
- 2026-04-14
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:41:51
| 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.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M020 | openfda.application_number | |
| brand name | Naturium Dew Glow Tinted Moisturizer SPF50-light | openfda.brand_name | |
| brand name | Naturium Dew Glow Tinted Moisturizer SPF50-medium | openfda.brand_name | |
| brand name | Naturium Dew Glow Tinted Moisturizer SPF50-deep | openfda.brand_name | |
| generic name | HOMOSALATE, OCTISALATE, AVOBENZONE | openfda.generic_name | |
| manufacturer name | PML NYC, LLC | openfda.manufacturer_name | |
| ndc | package | 59735-922-02 | openfda.package_ndc |
| ndc | package | 59735-923-02 | openfda.package_ndc |
| ndc | package | 59735-921-02 | openfda.package_ndc |
| ndc | product | 59735-923 | openfda.product_ndc |
| ndc | product | 59735-921 | openfda.product_ndc |
| ndc | product | 59735-922 | openfda.product_ndc |
| ndc11 | package | 59735092302 | derived:openfda.package_ndc |
| ndc11 | package | 59735092202 | derived:openfda.package_ndc |
| ndc11 | package | 59735092102 | derived:openfda.package_ndc |
| spl id | 4f782e36-b736-efc7-e063-6394a90adfda | id | |
| spl set id | 1c3489a6-5b98-2dc2-e063-6294a90a0695 | set_id | |
| unii | V06SV4M95S | openfda.unii | |
| unii | G63QQF2NOX | openfda.unii | |
| unii | 4X49Y0596W | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.