Home NDC 83252-118 BINDA Face and Body Sunscreen SPF50
Product NDC 83252-118
11-digit product format 832520118
Labeler code 83252
Product ID 83252-118_452bb793-827a-df74-e063-6394a90ade89
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 2025-06-25
Substance ZINC OXIDE
Active strength 25 kg/100kg
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 83252-118 83252-118-00 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 83252-118 83252-118-15 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 BINDA Face and Body Sunscreen SPF50
Listing expiration 2026-12-31 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 83252-118-00 BINDA Face and Body Sunscreen SPF50 0.11 kg in 1 BOTTLE, PUMP CREAM 0.11 2 83252-118-15 BINDA Face and Body Sunscreen SPF50 2 kg in 1 BOTTLE, PUMP CREAM 2 2 83252-118-21 BINDA Face and Body Sunscreen SPF50 1 kg in 1 BOTTLE, PUMP CREAM 1 2 83252-118-25 BINDA Face and Body Sunscreen SPF50 0.1 kg in 1 BOTTLE, PUMP CREAM 0.1 2
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 83252-118-00 83252011800 0.11 kg in 1 BOTTLE, PUMP 0.11 kg Historical 83252-118-15 83252011815 2 kg in 1 BOTTLE, PUMP 2 kg Historical 83252-118-21 83252011821 1 kg in 1 BOTTLE, PUMP (83252-118-21) 1 kg 2025-06-25 No No Current 83252-118-25 83252011825 .1 kg in 1 BOTTLE, PUMP (83252-118-25) 2025-12-05 No No Current