Home NDC 84803-111 ULTRA VIOLETTE SPF ON THE GLOW
Product NDC 84803-111
11-digit product format 848030111
Labeler code 84803
Product ID 84803-111_47b7dab4-2800-9cda-e063-6394a90a24da
Type HUMAN OTC DRUG
Nonproprietary name SPF 50
Dosage form KIT
Route TOPICAL
Labeler Grace And Fire USA Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-11-29
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 SPF ON THE GLOW
Brand name suffix Duo Pack Kit
Listing expiration 2027-12-31 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 84803-104-02 ULTRA VIOLETTE SPF ON THE GLOWDuo Pack Kit 15 g in 1 TUBE OINTMENT 1 g in 15 3 g in 100g 4 84803-111-01 ULTRA VIOLETTE SPF ON THE GLOWDuo Pack Kit 1 in 1 KIT KIT 1 4
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 26 of 357 · 7,139 matching rows.
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 30 ml Historical 84803-104-02 84803010402 15 g in 1 TUBE 15 g Historical 84803-111-01 84803011101 1 KIT in 1 KIT (84803-111-01) * 30 mL in 1 BOTTLE, SPRAY (84803-101-30) * 15 g in 1 TUBE (84803-104-02) 1 kit 2026-01-01 No No Current