Derma E Sun Defense Face

Product NDC
54108-0419
11-digit product format
541080419
Labeler code
54108
Product ID
54108-0419_dd9fabd4-2126-49ff-aa1a-1e696ad13c56
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide Titanium Dioxide
Dosage form
LOTION
Route
TOPICAL
Labeler
derma e
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-12-15
Substance
TITANIUM DIOXIDE; ZINC OXIDE
Active strength
26.4; 195 mg/g; mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Derma E Sun Defense Face
Brand name suffix
SPF 30
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TITANIUM DIOXIDE26.4 mg/g
ZINC OXIDE195 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii15FIX9V2JP, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54108-0419-1Derma E Sun Defense FaceSPF 3056 g in 1 TUBELOTION561
54108-0419-1Derma E Sun Defense FaceSPF 301 in 1 BOXLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54108-0419DERMA E SUN DEFENSE FACE SPF 30 (ZINC OXIDE TITANIUM DIOXIDE) LOTION [DERMA E]1Current NDC, 2 package rows20240719_d90b8f81-de7a-4022-800a-90f063e94180.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
54108-0419-1541080419011 TUBE in 1 BOX (54108-0419-1) / 56 g in 1 TUBE1 tube2022-12-15NoNoHistorical