Home NDC 59735-338 NATURIUM Dew-Glow Moisturizer SPF 50
Product NDC 59735-338
11-digit product format 597350338
Labeler code 59735
Product ID 59735-338_4f7828b7-bf2d-e4e7-e063-6294a90a3e0f
Type HUMAN OTC DRUG
Nonproprietary name NATURIUM Dew-Glow Moisturizer SPF 50
Dosage form CREAM
Route TOPICAL
Labeler PML NYC, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-11-01
Substance OCTISALATE; AVOBENZONE; HOMOSALATE
Active strength 5; 3; 10 g/mL; g/mL; g/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 SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 5 g/mL AVOBENZONE 3 g/mL HOMOSALATE 10 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup G63QQF2NOX Internal UNII lookup V06SV4M95S Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59735-338-01 NATURIUM Dew-Glow Moisturizer SPF 50 1 in 1 CARTON CREAM 1 4 59735-338-01 NATURIUM Dew-Glow Moisturizer SPF 50 50 mL in 1 TUBE CREAM 50 4 59735-338-03 NATURIUM Dew-Glow Moisturizer SPF 50 50 mL in 1 TUBE CREAM 50 4 59735-338-04 NATURIUM Dew-Glow Moisturizer SPF 50 1 in 1 CARTON CREAM 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59735-338 NATURIUM DEW-GLOW MOISTURIZER SPF 50 CREAM [MANA PRODUCTS, INC] 3 Current NDC, 4 package rows 20240823_00c93b11-754e-701c-e063-6294a90a3b1d.zip
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 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 59735-338-01 59735033801 1 TUBE in 1 CARTON (59735-338-01) / 50 mL in 1 TUBE 1 tube 2022-11-01 No No Current 59735-338-03 59735033803 50 mL in 1 TUBE 50 ml Historical 59735-338-04 59735033804 1 TUBE in 1 CARTON (59735-338-04) / 50 mL in 1 TUBE (59735-338-03) 1 tube 2022-11-01 No No Current