FDA.reportPublic FDA data

Moisturizing Sunscreen SPF 50

Product NDC
72476-954
11-digit product format
724760954
Labeler code
72476
Product ID
72476-954_4a2cd481-7363-9932-e063-6294a90aae1a
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate
Dosage form
LOTION
Route
TOPICAL
Labeler
Retail Business Service, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-12-19
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength
30; 120; 50 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
Moisturizing Sunscreen SPF 50
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE120 mg/mL
OCTISALATE50 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72476-954-05Moisturizing Sunscreen SPF 50207 mL in 1 TUBELOTION2075
72476-954-34Moisturizing Sunscreen SPF 50236 mL in 1 BOTTLELOTION2365

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72476-954MOISTURIZING SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE) LOTION [RETAIL BUSINESS SERVICE, LLC]4Current NDC, 2 package rows20250328_9de8b6b1-024b-4b71-96e6-fea68088d3ab.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72476-954-0572476095405207 mL in 1 TUBE (72476-954-05) 207 ml2025-03-26NoNoHistorical
72476-954-3472476095434236 mL in 1 BOTTLE (72476-954-34) 236 ml2023-12-19NoNoHistorical