Home NDC 84610-400 ANUA INVISIBLE MATTE FINISH SUNSCREEN
Product NDC 84610-400
11-digit product format 846100400
Labeler code 84610
Product ID 84610-400_48c81828-4da7-4704-e063-6394a90af97f
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler The Founders Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-14
Substance HOMOSALATE; OCTISALATE; AVOBENZONE; OCTOCRYLENE
Active strength 66; 45; 27; 50 mg/mL; 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 ANUA INVISIBLE MATTE FINISH SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 66 mg/mL OCTISALATE 45 mg/mL AVOBENZONE 27 mg/mL OCTOCRYLENE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 84610-400-01 ANUA INVISIBLE MATTE FINISH SUNSCREEN 50 mL in 1 TUBE CREAM 50 2 84610-400-01 ANUA INVISIBLE MATTE FINISH SUNSCREEN 1 in 1 CARTON CREAM 1 2
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 84610-400-01 84610040001 1 TUBE in 1 CARTON (84610-400-01) / 50 mL in 1 TUBE 1 tube 2025-11-14 No No Current