Home NDC 82733-294 SIMPLI DAY All In One SmartCream SPF 42
Product NDC 82733-294
11-digit product format 827330294
Labeler code 82733
Product ID 82733-294_09e32c60-2b83-0226-e063-6294a90a6a2f
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE, OCTISALATE, OCTOCRYLENE, ENSULIZOLE
Dosage form CREAM
Route TOPICAL
Labeler SIMPLI SKIN MD LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-05-20
Substance ZINC OXIDE; OCTISALATE; OCTOCRYLENE; ENSULIZOLE
Active strength 50; 50; 50; 40 mg/mL; mg/mL; mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 SIMPLI DAY All In One SmartCream SPF 42
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 50 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 50 mg/mL ENSULIZOLE 40 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 82733-294-00 SIMPLI DAY All In One SmartCream SPF 42 1 in 1 BOX CREAM 1 2 82733-294-00 SIMPLI DAY All In One SmartCream SPF 42 50 mL in 1 TUBE CREAM 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82733-294 SIMPLI DAY ALL IN ONE SMARTCREAM SPF 42 (ZINC OXIDE, OCTISALATE, OCTOCRYLENE, ENSULIZOLE) CREAM [SIMPLI SKIN MD LLC] 2 Current NDC, Legacy NDC, 2 package rows 20231112_e5aab0ec-eda2-4073-998a-966202dc2233.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 82733-294-00 82733029400 1 TUBE in 1 BOX (82733-294-00) / 50 mL in 1 TUBE 1 tube 2022-05-20 0000-00-00 No No Current