Home NDC 83252-144 OZE SUN BONDI
Product NDC 83252-144
11-digit product format 832520144
Labeler code 83252
Product ID 83252-144_47b1aaf5-2cba-43c9-e063-6394a90a4117
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide sunscreen
Dosage form CREAM
Route TOPICAL
Labeler VEGANIC SKN LIMITED
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-05
Substance ZINC OXIDE
Active strength 25 kg/100kg
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 OZE SUN BONDI
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 25 kg/100kg
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 83252-144-15 OZE SUN BONDI 2 kg in 1 BOTTLE, PUMP CREAM 2 1 83252-144-21 OZE SUN BONDI 1 kg in 1 BOTTLE, PUMP CREAM 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 83252-144-15 83252014415 2 kg in 1 BOTTLE, PUMP (83252-144-15) 2 kg 2026-01-05 No No Current 83252-144-21 83252014421 1 kg in 1 BOTTLE, PUMP (83252-144-21) 1 kg 2026-01-05 No No Current