FDA.reportPublic FDA data

Premium Moisturizing Sunscreen SPF 50

Product NDC
69039-234
11-digit product format
690390234
Labeler code
69039
Product ID
69039-234_0a2216c6-ceed-4dd6-e063-6294a90a5f30
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
SPRAY
Route
TOPICAL
Labeler
Sun Bum LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-08-09
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 150; 50; 70 mg/g; mg/g; 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
Premium Moisturizing Sunscreen SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/g
HOMOSALATE150 mg/g
OCTISALATE50 mg/g
OCTOCRYLENE70 mg/g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69039-234-01Premium Moisturizing Sunscreen SPF 50170 g in 1 CANSPRAY1705
69039-234-02Premium Moisturizing Sunscreen SPF 50142 g in 1 CANSPRAY1425

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69039-234PREMIUM MOISTURIZING SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [SUN BUM LLC]5Current NDC, Legacy NDC, 2 package rows20231115_f1d46728-6933-4e6f-b7c0-3613466aa1f0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69039-234-0169039023401170 g in 1 CAN (69039-234-01) 170 g2022-08-090000-00-00NoNoCurrent
69039-234-0269039023402142 g in 1 CAN (69039-234-02) 142 g2023-10-01NoNoCurrent