Home NDC 59735-922 Naturium Dew Glow Tinted Moisturizer SPF50-light
Product NDC 59735-922
11-digit product format 597350922
Labeler code 59735
Product ID 59735-922_4f782e36-b736-efc7-e063-6394a90adfda
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, Avobenzone
Dosage form LOTION
Route TOPICAL
Labeler PML NYC, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-12-27
Substance HOMOSALATE; AVOBENZONE; OCTISALATE
Active strength 10; 3; 5 g/50mL; g/50mL; g/50mL
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 Tinted Moisturizer SPF50-light
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 10 g/50mL AVOBENZONE 3 g/50mL OCTISALATE 5 g/50mL
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 59735-922-02 Naturium Dew Glow Tinted Moisturizer SPF50-light 50 mL in 1 TUBE LOTION 50 5 59735-922-02 Naturium Dew Glow Tinted Moisturizer SPF50-light 1 in 1 CARTON LOTION 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59735-922 NATURIUM DEW GLOW TINTED MOISTURIZER SPF50-DEEP (HOMOSALATE, OCTISALATE, AVOBENZONE) LOTION NATURIUM DEW GLOW TINTED MOISTURIZER SPF50-MEDIUM (HOMOSALATE, OCTISALATE, AVOBENZONE) LOTION NATURIUM DEW GLOW TINTED MOISTURIZER SPF50-LIGHT (HOMOSALATE, OCTISALATE, AVOBENZONE) LOTION [MANA PRODUCTS, INC.] 4 Current NDC, 2 package rows 20240703_1c3489a6-5b98-2dc2-e063-6294a90a0695.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 59735-922-02 59735092202 1 TUBE in 1 CARTON (59735-922-02) / 50 mL in 1 TUBE 1 tube 2023-12-27 No No Current