Home NDC 84803-101 Ultra Violette Preen Screen Broad Spectrum SPF 50
Product NDC 84803-101
11-digit product format 848030101
Labeler code 84803
Product ID 84803-101_533cb134-43ee-e843-e063-6294a90a38a1
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 OCTISALATE; OCTOCRYLENE; HOMOSALATE; AVOBENZONE
Active strength 50; 60; 100; 30 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 Ingredient Strength OCTISALATE 50 mg/mL OCTOCRYLENE 60 mg/mL HOMOSALATE 100 mg/mL AVOBENZONE 30 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84803-101-30 ULTRA VIOLETTE SPF ON THE GLOWDuo Pack Kit 30 mL in 1 BOTTLE, SPRAY SPRAY 1 mL in 30 30 mg in 1mL 4 84803-101-30 Ultra Violette Preen Screen Broad Spectrum SPF 50 30 mL in 1 BOTTLE, SPRAY SPRAY 30 2 84803-101-50 Ultra Violette Preen Screen Broad Spectrum SPF 50 50 mL in 1 BOTTLE, SPRAY SPRAY 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84803-101 ULTRA VIOLETTE PREEN SCREEN BROAD SPECTRUM SPF 50 (AVONBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE) SPRAY [GRACE AND FIRE USA INC.] 1 Current NDC, 2 package rows 20241202_26a0fc0d-a903-2ac1-e063-6394a90a13db.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 120 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Daily Skin Protection Sunscreen NT ZINC OXIDE SKINPLUSBYOROYO LLC 35a94d6f-9b1c-1b26-e063-6394a90abe65 2025-12-15 Exact identifier application number: M020 Daily Skin Protection Sunscreen NT ZINC OXIDE SKINPLUSBYOROYO LLC 35a9a6ed-c446-c90c-e063-6294a90aaa74 2025-12-15 Exact identifier application number: M020 Daily Skin Protection Sunscreen Tinted ZINC OXIDE SKINPLUSBYOROYO LLC 35a9ecd7-b416-0aab-e063-6294a90a323d 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer NT TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 3596fe93-836b-4f8e-e063-6294a90a674a 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 359723bb-6152-9566-e063-6294a90a59e0 2025-12-15 Exact identifier application number: M020 Daily Skin Protection Sunscreen Tinted ZINC OXIDE SKINPLUSBYOROYO LLC 35aa194a-9a2e-2b5f-e063-6294a90a9877 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer NT TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 3596cd73-0811-32bc-e063-6394a90ad132 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 359782d7-6601-7d96-e063-6394a90af9dc 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETICS BY RIKI LLC 37f1b692-0b80-0536-e063-6294a90ae863 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETICS BY RIKI LLC 387d5194-bc12-68c1-e063-6394a90ab152 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387c23c2-a9f0-f484-e063-6394a90a4104 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387be96f-8cda-ce02-e063-6394a90abea5 2025-12-15 Exact identifier application number: M020 Serum Lightly Tinted ZINC OXIDE PANDA PAMPERING LLC 387c593b-c65b-62b5-e063-6294a90ac4c2 2025-12-15 Exact identifier application number: M020 Serum Lightly Tinted ZINC OXIDE PANDA PAMPERING LLC 387c9167-638c-1e30-e063-6394a90a9374 2025-12-15 Exact identifier application number: M020 REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37ede476-43b6-a7c8-e063-6294a90a3e8f 2025-12-15 Exact identifier application number: M020 REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37efa5e1-e88e-d251-e063-6394a90a9371 2025-12-15 Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd330bf-92e4-3664-e063-6294a90a0475 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd37dd1-fd43-7af4-e063-6394a90ae3a0 2025-12-15 Warnings Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd3dcab-e9fb-0ef5-e063-6394a90acef1 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd40a6a-d52e-ab87-e063-6294a90a966e 2025-12-15 Warnings Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84803-101-30 84803010130 30 mL in 1 BOTTLE, SPRAY (84803-101-30) 30 ml 2024-12-01 No No Current 84803-101-50 84803010150 50 mL in 1 BOTTLE, SPRAY (84803-101-50) 50 ml 2024-12-01 No No Current