Home NDC 51326-879 Moisturizing Antioxidant
Product NDC 51326-879
11-digit product format 513260879
Labeler code 51326
Product ID 51326-879_22e498d9-1e2e-48a6-a3c6-87a0dca750a3
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate, Octisalate, Homosalate, Oxybenzone, Zinc Oxide
Dosage form SPRAY
Route TOPICAL
Labeler Topiderm, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance OCTISALATE; OCTINOXATE; OXYBENZONE; HOMOSALATE; ZINC OXIDE
Active strength 50; 75; 50; 70; 60 mg/mL; 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 Moisturizing Antioxidant
Brand name suffix SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 50 mg/mL OCTINOXATE 75 mg/mL OXYBENZONE 50 mg/mL HOMOSALATE 70 mg/mL ZINC OXIDE 60 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51326-879-01 Moisturizing AntioxidantSPF 50 120 mL in 1 CANISTER SPRAY 120 1
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 51326-879-01 51326087901 120 mL in 1 CANISTER (51326-879-01) 120 ml 2020-01-01 No No Current