Home NDC 76354-300 Naturium Dew Glow Moisturizer Mineral SPF 50
Product NDC 76354-300
11-digit product format 763540300
Labeler code 76354
Product ID 76354-300_535f64d1-5ef3-92b4-e063-6294a90a0f0c
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler e.l.f. Cosmetics, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-02
Substance ZINC OXIDE
Active strength 100 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Naturium Dew Glow Moisturizer Mineral SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 100 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 76354-300-01 76354030001 1 TUBE in 1 BOX (76354-300-01) / 50 mL in 1 TUBE 1 tube 2026-02-02 No No Current