Home NDC 72935-003 Neora
Product NDC 72935-003
11-digit product format 729350003
Labeler code 72935
Product ID 72935-003_08698eda-076f-5919-e063-6294a90a1fa2
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form GEL
Route TOPICAL
Labeler Neora, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-07-01
Substance OCTISALATE; AVOBENZONE; HOMOSALATE
Active strength 5; 3; 9.5 g/100mL; g/100mL; g/100mL
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 Neora
Brand name suffix Age IQ Invisi-Bloc Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 5 g/100mL AVOBENZONE 3 g/100mL HOMOSALATE 9.5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup G63QQF2NOX Internal UNII lookup V06SV4M95S Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72935-003-30 NeoraAge IQ Invisi-Bloc Sunscreen 30 mL in 1 TUBE GEL 30 2 72935-003-30 NeoraAge IQ Invisi-Bloc Sunscreen 1 in 1 CARTON GEL 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72935-003 NEORA AGE IQ INVISI-BLOC SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) GEL [NEORA, LLC] 2 Current NDC, 2 package rows 20231024_f2f3601f-081a-4bae-e053-2a95a90a4fac.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 72935-003-30 72935000330 1 TUBE in 1 CARTON (72935-003-30) / 30 mL in 1 TUBE 1 tube 2023-07-01 No No Current