Cell Fusion C Derma UV Mineral Sunscreen Broad Spectrum SPF 50

Product NDC
52554-9064
11-digit product format
525549064
Labeler code
52554
Product ID
52554-9064_2e5c2af4-f033-aefe-e063-6394a90aa7b0
Type
HUMAN OTC DRUG
Nonproprietary name
Homosalate, Octisalate, Octocrylene, Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
CMS LAB Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-02-14
Substance
ZINC OXIDE
Active strength
19 g/50mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Cell Fusion C Derma UV Mineral Sunscreen Broad Spectrum SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE19 g/50mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52554-9064-1Cell Fusion C Derma UV Mineral Sunscreen Broad Spectrum SPF 5050 mL in 1 TUBECREAM501
52554-9064-1Cell Fusion C Derma UV Mineral Sunscreen Broad Spectrum SPF 501 in 1 BOXCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52554-9064CELL FUSION C DERMA UV MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 (HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE) CREAM [CMS LAB INC.]1Current NDC, 2 package rows20250221_2e5c2add-8ed0-a990-e063-6394a90a87ea.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
52554-9064-1525549064011 TUBE in 1 BOX (52554-9064-1) / 50 mL in 1 TUBE1 tube2025-02-14NoNoHistorical