Home NDC 69473-019 Alumier MD Post Procedure Kit
Product NDC 69473-019
11-digit product format 694730019
Labeler code 69473
Product ID 69473-019_252859de-6675-5e07-e063-6394a90a64a1
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form KIT
Route TOPICAL
Labeler Alumier Labs
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-10-23
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 Post Procedure Kit
Listing expiration 2026-12-31 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 69473-019-01 Alumier MD Post Procedure Kit 1 in 1 CARTON KIT 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69473-019 ALUMIER MD POST PROCEDURE KIT (TITANIUM DIOXIDE, ZINC OXIDE) KIT [ALUMIER LABS] 1 Current NDC, 1 package rows 20241025_252859de-6676-5e07-e063-6394a90a64a1.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 Sample Exclude flag Status 69473-019-01 69473001901 1 KIT in 1 CARTON (69473-019-01) * 15 mL in 1 TUBE * 15 mL in 1 TUBE * 15 mL in 1 TUBE 1 kit 2024-10-23 No No Current