Home NDC 69219-111 PerfecTint Powder SPF 40
Product NDC 69219-111
11-digit product format 692190111
Labeler code 69219
Product ID 69219-111_2b4f67e8-6793-c22e-e063-6394a90ac9ac
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form POWDER
Route TOPICAL
Labeler Science of Skincare
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-12-19
Substance ZINC OXIDE
Active strength 25 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 69219-111 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 69219-111 69219-111-11 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 69219-111 69219-111-01 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 PerfecTint Powder SPF 40
Brand name suffix All Shades
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 25 g/100g
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 69219-111-01 PerfecTint Powder SPF 40All Shades 3.5 g in 1 BOTTLE, PLASTIC POWDER 3.5 4 69219-111-11 PerfecTint Powder SPF 40All Shades 1 in 1 BOX POWDER 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69219-111 PERFECTINT POWDER SPF 40 ALL SHADES (ZINC OXIDE) POWDER [SCIENCE OF SKINCARE] 4 Current NDC, 2 package rows 20250112_bb26c010-299e-3dc5-e053-2995a90a2c89.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 69219-111-01 69219011101 3.5 g in 1 BOTTLE, PLASTIC (69219-111-01) 3.5 g 2023-12-19 No No Current 69219-111-11 69219011111 1 BOTTLE, PLASTIC in 1 BOX (69219-111-11) / 3.5 g in 1 BOTTLE, PLASTIC (69219-111-01) 2023-12-19 No No Current