Home NDC 69219-112 LiProtect SPF 35
Product NDC 69219-112
11-digit product format 692190112
Labeler code 69219
Product ID 69219-112_2cdc21b4-a379-9c3a-e063-6294a90a829b
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Titanium Dioxide
Dosage form STICK
Route TOPICAL
Labeler Science of Skincare
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-12-31
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 10.2; 1 g/100g; g/100g
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 · 3 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 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 69219-112 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 69219-112 69219-112-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 69219-112 69219-112-11 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 LiProtect SPF 35
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 10.2 g/100g TITANIUM DIOXIDE 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69219-112-01 LiProtect SPF 35 5 g in 1 BOTTLE, PLASTIC STICK 5 3 69219-112-11 LiProtect SPF 35 1 in 1 BOX STICK 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69219-112 LIPROTECT SPF 35 (ZINC OXIDE, TITANIUM DIOXIDE) STICK [SCIENCE OF SKINCARE] 3 Current NDC, 2 package rows 20250130_0d0a2657-4098-3c60-e063-6294a90acabb.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 45 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 69219-112-01 69219011201 5 g in 1 BOTTLE, PLASTIC (69219-112-01) 5 g 2023-12-31 No No Current 69219-112-11 69219011211 1 BOTTLE, PLASTIC in 1 BOX (69219-112-11) / 5 g in 1 BOTTLE, PLASTIC (69219-112-01) 2023-12-31 No No Current