Derma B Everyday Fit Sunscreen SPF 50

Product NDC
51141-0701
11-digit product format
511410701
Labeler code
51141
Product ID
51141-0701_4a0024d0-7a49-7495-e063-6394a90a9371
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBEZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
LOTION
Route
TOPICAL
Labeler
NeoPharm Co., Ltd.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-12-15
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 95; 45; 60 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Derma B Everyday Fit Sunscreen SPF 50
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE95 mg/mL
OCTISALATE45 mg/mL
OCTOCRYLENE60 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51141-0701-5Derma B Everyday Fit Sunscreen SPF 5050 mL in 1 TUBELOTION502

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
51141-0701-55114107010550 mL in 1 TUBE (51141-0701-5) 50 ml2025-12-15NoNoCurrent