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

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

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
84803-104-02ULTRA VIOLETTE SPF ON THE GLOWDuo Pack Kit15 g in 1 TUBEOINTMENT1 g in 153 g in 100g4
84803-111-01ULTRA VIOLETTE SPF ON THE GLOWDuo Pack Kit1 in 1 KITKIT14

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84803-101-308480301013030 mL in 1 BOTTLE, SPRAY30 mlHistorical
84803-104-028480301040215 g in 1 TUBE15 gHistorical
84803-111-01848030111011 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 kit2026-01-01NoNoCurrent