EGF FGF DNA UV SHIELD

Product NDC
58831-1100
11-digit product format
588311100
Labeler code
58831
Product ID
58831-1100_286c245e-8eac-2cd4-e063-6394a90ab01f
Type
HUMAN OTC DRUG
Nonproprietary name
Ethylhexyl Methoxycinnamate, Titanium Dioxide, Ethylhexyl Salicylate
Dosage form
CREAM
Route
TOPICAL
Labeler
Dermaesthetics Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-10-01
Substance
OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
Active strength
3.24; 2.04; 3 g/60mL; g/60mL; g/60mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
EGF FGF DNA UV SHIELD
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTINOXATE3.24 g/60mL
OCTISALATE2.04 g/60mL
TITANIUM DIOXIDE3 g/60mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4Y5P7MUD51, 4X49Y0596W, 15FIX9V2JP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58831-1100-1EGF FGF DNA UV SHIELD60 mL in 1 TUBECREAM606
58831-1100-2EGF FGF DNA UV SHIELD1 in 1 CARTONCREAM16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58831-1100EGF FGF DNA UV SHIELD (ETHYLHEXYL METHOXYCINNAMATE, TITANIUM DIOXIDE, ETHYLHEXYL SALICYLATE) CREAM [DERMAESTHETICS INC.]6Current NDC, Legacy NDC, 2 package rows20241207_13e2630d-9915-4287-91fd-deb672150131.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58831-1100-15883111000160 mL in 1 TUBE60 mlHistorical
58831-1100-2588311100021 TUBE in 1 CARTON (58831-1100-2) / 60 mL in 1 TUBE (58831-1100-1) 1 tube2021-10-010000-00-00NoNoCurrent