FDA.reportPublic FDA data

AGE20S SUNSCREEN DUO

Product NDC
67225-5333
11-digit product format
672255333
Labeler code
67225
Product ID
67225-5333_4eef170d-8ffc-0fc1-e063-6394a90a908c
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide, Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
KIT
Route
TOPICAL
Labeler
Aekyung Industrial Co., Ltd.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-04-08
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
AGE20S SUNSCREEN DUO
Listing expiration
2027-12-31

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67225-5033-1AGE20S SUNSCREEN DUO50 g in 1 TUBECREAM50 g4.5 g in 50g1
67225-5033-2AGE20S SUNSCREEN DUO1 in 1 BOXCREAM4.5 g in 50g1
67225-5301-4AGE20S SUNSCREEN DUO50 g in 1 TUBECREAM50 g7.34 g in 50g1
67225-5301-5AGE20S SUNSCREEN DUO1 in 1 BOXCREAM7.34 g in 50g1
67225-5333-1AGE20S SUNSCREEN DUO1 in 1 CARTONKIT11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
67225-5033-16722550330150 g in 1 TUBE50 gHistorical
67225-5033-2672255033021 in 1 BOXHistorical
67225-5301-46722553010450 g in 1 TUBE50 gHistorical
67225-5301-5672255301051 in 1 BOXHistorical
67225-5333-1672255333011 KIT in 1 CARTON (67225-5333-1) * 1 TUBE in 1 BOX (67225-5301-5) / 50 g in 1 TUBE (67225-5301-4) * 1 TUBE in 1 BOX (67225-5033-2) / 50 g in 1 TUBE (67225-5033-1) 1 kit2026-04-08NoNoHistorical