Home NDC 82800-080 Prequel Lip Visor SPF 30 ROSEDUST
Product NDC 82800-080
11-digit product format 828000080
Labeler code 82800
Product ID 82800-080_45200a46-7577-78f4-e063-6294a90a3580
Type HUMAN OTC DRUG
Nonproprietary name Lip 30 Clear
Dosage form LIQUID
Route TOPICAL
Labeler The Center Brands, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-28
Substance AVOBENZONE; OCTINOXATE
Active strength 3; 7.5 mg/100mg; mg/100mg
NDC exclude flag No
Listing certified through 2026-12-31
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 Prequel Lip Visor SPF 30 ROSEDUST
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 mg/100mg OCTINOXATE 7.5 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup
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 82800-080-01 Prequel Lip Visor SPF 30 ROSEDUST 10 mg in 1 TUBE LIQUID 10 2 82800-080-01 Prequel Lip Visor SPF 30 ROSEDUST 1 in 1 PACKAGE LIQUID 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82800-080 PREQUEL LIP VISOR SPF 30 ROSEDUST (LIP 30 CLEAR) LIQUID [THE CENTER BRANDS, LLC] 1 Current NDC, 2 package rows 20250429_33d5e1ad-ba7a-25f8-e063-6294a90aa38e.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 109 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 82800-080-01 82800008001 1 TUBE in 1 PACKAGE (82800-080-01) / 10 mg in 1 TUBE 1 tube 2025-04-28 No No Current