Quick Screen Sunscreen SPF 50

Product NDC
82654-000
11-digit product format
826540000
Labeler code
82654
Product ID
82654-000_2df51c1a-9783-0d8f-e063-6394a90afefb
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
LOTION
Route
TOPICAL
Labeler
The Quick Flick PTY LTD
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-06-15
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 50; 80 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Quick Screen Sunscreen SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE80 mg/mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82654-000-01Quick Screen Sunscreen SPF 501 in 1 BOXLOTION13
82654-000-01Quick Screen Sunscreen SPF 5090 mL in 1 BOTTLE, SPRAYLOTION903

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82654-000QUICK SCREEN SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [THE QUICK FLICK PTY LTD]3Current NDC, 2 package rows20250214_3788666e-7efa-43da-95f5-6218b7fcb6ea.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
82654-000-01826540000011 BOTTLE, SPRAY in 1 BOX (82654-000-01) / 90 mL in 1 BOTTLE, SPRAY2023-06-15NoNoHistorical