Home NDC 52915-030 SPF30 EVERYDAY/YEAR-ROUND SUNSCREEN
Product NDC 52915-030
11-digit product format 529150030
Labeler code 52915
Product ID 52915-030_2edb97ba-b338-4778-9116-c8218f5679f3
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE
Dosage form LOTION/SHAMPOO
Route TOPICAL
Labeler ORGANIC & SUSTAINABLE BEAUTY
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-08-31
Substance TITANIUM DIOXIDE
Active strength 120 mg/g
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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 52915-030-29 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 52915-030-29 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 52915-030-29 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
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 SPF30 EVERYDAY/YEAR-ROUND SUNSCREEN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 120 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52915-030-29 SPF30 EVERYDAY/YEAR-ROUND SUNSCREEN 82 g in 1 TUBE LOTION/SHAMPOO 82 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52915-030 SPF30 EVERYDAY/YEAR-ROUND SUNSCREEN (TITANIUM DIOXIDE) LOTION/SHAMPOO [ORGANIC & SUSTAINABLE BEAUTY] 5 Current NDC, Legacy NDC, 1 package rows 20241109_547388c6-378b-488b-89d1-c77ebc5d2ed8.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 162 of 353 · 7,041 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 52915-030-29 52915003029 82 g in 1 TUBE (52915-030-29) 82 g 2015-08-31 0000-00-00 No No Current