Home NDC 53208-741 belif Dew guard - milky sun serum Broad Spectrum SPF 40 sunscreen
Product NDC 53208-741
11-digit product format 532080741
Labeler code 53208
Product ID 53208-741_308e517a-92f0-65a5-e063-6294a90a58b3
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler LG H&H CO., LTD.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-11
Substance HOMOSALATE; AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength 9; 2.7; 4.5; 9 g/100g; g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
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 belif Dew guard - milky sun serum Broad Spectrum SPF 40 sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 9 g/100g AVOBENZONE 2.7 g/100g OCTISALATE 4.5 g/100g OCTOCRYLENE 9 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53208-741-01 belif Dew guard - milky sun serum Broad Spectrum SPF 40 sunscreen 50 g in 1 BOTTLE, PLASTIC CREAM 50 2 53208-741-02 belif Dew guard - milky sun serum Broad Spectrum SPF 40 sunscreen 1 in 1 CARTON CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53208-741 BELIF DEW GUARD - MILKY SUN SERUM BROAD SPECTRUM SPF 40 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM BELIF DEW GUARD - GLOW BOOST SERUM BROAD SPECTRUM SPF 40 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM [LG H&H CO., LTD.] 2 Current NDC, 2 package rows 20250411_2b38da59-b83e-4285-e063-6294a90ac6a7.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 53208-741-01 53208074101 50 g in 1 BOTTLE, PLASTIC 50 g Historical 53208-741-02 53208074102 1 BOTTLE, PLASTIC in 1 CARTON (53208-741-02) / 50 g in 1 BOTTLE, PLASTIC (53208-741-01) 2025-04-11 No No Current