Home NDC 69473-014 Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Amber
Product NDC 69473-014
11-digit product format 694730014
Labeler code 69473
Product ID 69473-014_28689862-f8cc-5f28-e063-6294a90ac654
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE, TITANIUM DIOXIDE
Dosage form LOTION
Route TOPICAL
Labeler Alumier Labs
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-02-04
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 90; 83 mg/mL; mg/mL
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 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 Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Amber
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 90 mg/mL TITANIUM DIOXIDE 83 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z 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 69473-014-01 Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Amber 60 mL in 1 TUBE LOTION 60 5 69473-014-01 Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Amber 1 in 1 CARTON LOTION 1 5 69473-014-02 Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Amber 8 mL in 1 TUBE LOTION 8 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69473-014 ALUMIER MD MOISTURE MATTE BROAD SPECTRUM SPF 40 SUNSCREEN AMBER (ZINC OXIDE, TITANIUM DIOXIDE) LOTION ALUMIER MD MOISTURE MATTE BROAD SPECTRUM SPF 40 SUNSCREEN SAND (ZINC OXIDE, TITANIUM DIOXIDE) LOTION ALUMIER MD MOISTURE MATTE BROAD SPECTRUM SPF 40 SUNSCREEN IVORY (ZINC OXIDE, TITANIUM DIOXIDE) LOTION [ALUMIER LABS] 5 Current NDC, Legacy NDC, 3 package rows 20241206_ba864a08-e66d-d286-e053-2995a90a1854.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 26 of 357 · 7,139 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 69473-014-01 69473001401 1 TUBE in 1 CARTON (69473-014-01) / 60 mL in 1 TUBE 1 tube 2021-02-04 0000-00-00 No No Current 69473-014-02 69473001402 8 mL in 1 TUBE (69473-014-02) 8 ml 2021-02-04 0000-00-00 No No Current