SPF 30 SUNSCREEN

Product NDC
53942-002
11-digit product format
539420002
Labeler code
53942
Product ID
53942-002_24b1cb9d-2eef-b05f-e063-6394a90a8c33
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
DEMOULAS SUPER MARKETS, INC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-02-25
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 50; 20 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
SPF 30 SUNSCREEN
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/g
HOMOSALATE100 mg/g
OCTISALATE50 mg/g
OCTOCRYLENE20 mg/g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53942-002-37SPF 30 SUNSCREEN156 g in 1 CANAEROSOL, SPRAY1566

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53942-002SPF 30 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) AEROSOL, SPRAY [DEMOULAS SUPER MARKETS, INC]6Current NDC, Legacy NDC, 1 package rows20241019_5ce3e436-37d1-4918-bb14-0be33b0bc86a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53942-002-3753942000237156 g in 1 CAN (53942-002-37) 156 g2012-03-100000-00-00NoNoCurrent