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

Additional Listing Data#

Finished product
Yes
Brand name base
Alumier MD Post Procedure Kit
Listing expiration
2026-12-31

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69473-019-01Alumier MD Post Procedure Kit1 in 1 CARTONKIT11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69473-019ALUMIER MD POST PROCEDURE KIT (TITANIUM DIOXIDE, ZINC OXIDE) KIT [ALUMIER LABS]1Current NDC, 1 package rows20241025_252859de-6676-5e07-e063-6394a90a64a1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69473-019-01694730019011 KIT in 1 CARTON (69473-019-01) * 15 mL in 1 TUBE * 15 mL in 1 TUBE * 15 mL in 1 TUBE1 kit2024-10-23NoNoHistorical