Home NDC 80573-089 Plius Daily SPF Moisturizer SPF 30
Product NDC 80573-089
11-digit product format 805730089
Labeler code 80573
Product ID 80573-089_48c0c6c7-dfa3-d42d-e063-6394a90a024e
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, OCTISALATE, OCTOCRYLENE
Dosage form CREAM
Route TOPICAL
Labeler PLIUS, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-14
Substance AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength 30; 50; 80 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 Plius Daily SPF Moisturizer SPF 30
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 80 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup 4X49Y0596W Internal UNII lookup 5A68WGF6WM 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 80573-089-30 Plius Daily SPF Moisturizer SPF 30 1 in 1 CARTON CREAM 1 4 80573-089-30 Plius Daily SPF Moisturizer SPF 30 30 mL in 1 TUBE CREAM 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80573-089 PLIUS DAILY SPF MOISTURIZER SPF 30 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) CREAM [PLIUS, INC] 3 Current NDC, Legacy NDC, 2 package rows 20231106_31866de9-afa0-4c11-be65-b61373551493.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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 80573-089-30 80573008930 1 TUBE in 1 CARTON (80573-089-30) / 30 mL in 1 TUBE 1 tube 2020-09-14 0000-00-00 No No Current