Home NDC 85260-282 Sonni SunDay Serum
Product NDC 85260-282
11-digit product format 852600282
Labeler code 85260
Product ID 85260-282_419d3622-3cf2-b28f-e063-6394a90a5ba5
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Sonni
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-28
Substance ZINC OXIDE
Active strength 132 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 Sonni SunDay Serum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 132 mg/mL
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 85260-282-01 Sonni SunDay Serum 50 mL in 1 BOTTLE, DROPPER LOTION 50 1 85260-282-02 Sonni SunDay Serum 1 in 1 CARTON LOTION 1 1
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 Sample Exclude flag Status 85260-282-01 85260028201 50 mL in 1 BOTTLE, DROPPER 50 ml Historical 85260-282-02 85260028202 1 BOTTLE, DROPPER in 1 CARTON (85260-282-02) / 50 mL in 1 BOTTLE, DROPPER (85260-282-01) 2025-08-28 No No Current