Home NDC 82404-101 LUXURY SUN RITUAL
Product NDC 82404-101
11-digit product format 824040101
Labeler code 82404
Product ID 82404-101_47d86fa0-0c4d-3b34-e063-6294a90a1eee
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler JANE STREET LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-05-01
Substance ZINC OXIDE
Active strength 10 g/100mL
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 LUXURY SUN RITUAL
Brand name suffix PORE SMOOTHING SPF 30 SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 10 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82404-101-11 LUXURY SUN RITUALPORE SMOOTHING SPF 30 SUNSCREEN 50 mL in 1 TUBE LOTION 50 4 82404-101-12 LUXURY SUN RITUALPORE SMOOTHING SPF 30 SUNSCREEN 1 in 1 BOX LOTION 1 4 82404-101-13 LUXURY SUN RITUALPORE SMOOTHING SPF 30 SUNSCREEN 3 mL in 1 TUBE LOTION 3 4 82404-101-14 LUXURY SUN RITUALPORE SMOOTHING SPF 30 SUNSCREEN 25 mL in 1 TUBE LOTION 25 4 82404-101-15 LUXURY SUN RITUALPORE SMOOTHING SPF 30 SUNSCREEN 1 in 1 BOX LOTION 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82404-101 LUXURY SUN RITUAL PORE SMOOTHING SPF 30 SUNSCREEN (ZINC OXIDE) LOTION [JANE STREET LLC] 3 Current NDC, Legacy NDC, 5 package rows 20231207_dbdd3e6a-f09d-90cf-e053-2a95a90a98a0.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 81 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 82404-101-11 82404010111 50 mL in 1 TUBE 50 ml Historical 82404-101-12 82404010112 1 TUBE in 1 BOX (82404-101-12) / 50 mL in 1 TUBE (82404-101-11) 1 tube 2022-05-01 0000-00-00 No No Current 82404-101-13 82404010113 3 mL in 1 TUBE (82404-101-13) 3 ml 2022-05-01 0000-00-00 Yes No Current 82404-101-14 82404010114 25 mL in 1 TUBE 25 ml Historical 82404-101-15 82404010115 1 TUBE in 1 BOX (82404-101-15) / 25 mL in 1 TUBE (82404-101-14) 1 tube 2022-12-01 0000-00-00 No No Current