Home NDC 51150-631 LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM
Product NDC 51150-631
11-digit product format 511500631
Labeler code 51150
Product ID 51150-631_51db9049-0cf7-4fab-e063-6294a90a7068
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide and Zinc Oxide
Dosage form LIQUID
Route TOPICAL
Labeler SICOS ET CIE
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-01
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 26.6; 153.5 mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 26.6 mg/mL ZINC OXIDE 153.5 mg/mL
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 SOI2LOH54Z Internal UNII lookup
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 51150-631-01 LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM 50 mL in 1 BOTTLE, PLASTIC LIQUID 50 2 51150-631-01 LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM 1 in 1 CARTON LIQUID 1 2 51150-631-02 LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM 30 mL in 1 JAR LIQUID 30 2 51150-631-02 LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM 1 in 1 CARTON LIQUID 1 2
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 128 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 51150-631-01 51150063101 1 BOTTLE, PLASTIC in 1 CARTON (51150-631-01) / 50 mL in 1 BOTTLE, PLASTIC 2026-04-01 No No Current 51150-631-02 51150063102 1 JAR in 1 CARTON (51150-631-02) / 30 mL in 1 JAR 1 jar 2026-05-15 No No Current