Ultra Violette Preen Screen Broad Spectrum SPF 50

Product NDC
84803-101
11-digit product format
848030101
Labeler code
84803
Product ID
84803-101_47aa0f01-e76c-44d4-e063-6394a90afe4b
Type
HUMAN OTC DRUG
Nonproprietary name
AVONBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE
Dosage form
SPRAY
Route
TOPICAL
Labeler
Grace and Fire USA Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-12-01
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 50; 60 mg/mL; 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
Ultra Violette Preen Screen Broad Spectrum SPF 50
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE60 mg/mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84803-101-30ULTRA VIOLETTE SPF ON THE GLOWDuo Pack Kit30 mL in 1 BOTTLE, SPRAYSPRAY1 mL in 3030 mg in 1mL4
84803-101-30Ultra Violette Preen Screen Broad Spectrum SPF 5030 mL in 1 BOTTLE, SPRAYSPRAY302
84803-101-50Ultra Violette Preen Screen Broad Spectrum SPF 5050 mL in 1 BOTTLE, SPRAYSPRAY502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84803-101ULTRA VIOLETTE PREEN SCREEN BROAD SPECTRUM SPF 50 (AVONBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE) SPRAY [GRACE AND FIRE USA INC.]1Current NDC, 2 package rows20241202_26a0fc0d-a903-2ac1-e063-6394a90a13db.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84803-101-308480301013030 mL in 1 BOTTLE, SPRAY (84803-101-30) 30 ml2024-12-01NoNoCurrent
84803-101-508480301015050 mL in 1 BOTTLE, SPRAY (84803-101-50) 50 ml2024-12-01NoNoCurrent