Home NDC 49967-767 LOreal Paris Skin Paradise Water Infused Tinted Moisturizer Broad Spectrum SPF 19 Sunscreen
Product NDC 49967-767
11-digit product format 499670767
Labeler code 49967
Product ID 49967-767_d20a0ca4-a16a-4e37-b59e-db8f02985012
Type HUMAN OTC DRUG
Nonproprietary name Ensulizole
Dosage form LIQUID
Route TOPICAL
Labeler L'Oreal USA Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-11-01
Substance ENSULIZOLE
Active strength 35 mg/mL
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 LOreal Paris Skin Paradise Water Infused Tinted Moisturizer Broad Spectrum SPF 19 Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ENSULIZOLE 35 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9YQ9DI1W42 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 49967-767-01 LOreal Paris Skin Paradise Water Infused Tinted Moisturizer Broad Spectrum SPF 19 Sunscreen 30 mL in 1 TUBE LIQUID 30 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-767 LOREAL PARIS SKIN PARADISE WATER INFUSED TINTED MOISTURIZER BROAD SPECTRUM SPF 19 SUNSCREEN (ENSULIZOLE) LIQUID [L'OREAL USA PRODUCTS INC] 6 Current NDC, Legacy NDC, 1 package rows 20240102_913116de-1abf-4844-8611-1db1b093ad00.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 Marketing end Sample Exclude flag Status 49967-767-01 49967076701 30 mL in 1 TUBE (49967-767-01) 30 ml 2020-11-01 0000-00-00 No No Current