Home NDC 82329-247 WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20
Product NDC 82329-247
11-digit product format 823290247
Labeler code 82329
Product ID 82329-247_09e3018f-8541-2069-e063-6394a90ad672
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE
Dosage form CREAM
Route TOPICAL
Labeler SKINMETICS INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-11-01
Substance OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE
Active strength 60; 30; 30 mg/mL; mg/mL; 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 WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 60 mg/mL OXYBENZONE 30 mg/mL TITANIUM DIOXIDE 30 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 95OOS7VE0Y Internal UNII lookup 15FIX9V2JP 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 82329-247-00 WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20 105 mL in 1 TUBE CREAM 105 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82329-247 WILMA SCHUMANN MOISTURE PROTEKTIV DAY CREAM SPF-20 (OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE) CREAM [SKINMETICS INC] 2 Current NDC, Legacy NDC, 1 package rows 20231112_4a719986-d1d0-4156-b803-04004b721504.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 82329-247-00 82329024700 105 mL in 1 TUBE (82329-247-00) 105 ml 2021-11-01 0000-00-00 No No Current