Home NDC 87489-002 VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen
Product NDC 87489-002
11-digit product format 874890002
Labeler code 87489
Product ID 87489-002_58819ee5-d014-c827-e063-6294a90a0570
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Octinoxate
Dosage form CREAM
Route TOPICAL
Labeler LCM TECHNOLOGY Co., Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-11
Substance TITANIUM DIOXIDE; ETHYLHEXYL METHOXYCINNAMATE
Active strength 1.35; 7.5 g/100g; g/100g
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 VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 1.35 g/100g ETHYLHEXYL METHOXYCINNAMATE 7.5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup 4Y5P7MUD51 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 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 87489-002-02 87489000202 1 TUBE in 1 BOX (87489-002-02) / 40 g in 1 TUBE (87489-002-01) 1 tube 2026-03-11 No No Current