Home NDC 79950-019 Bondi Sands SPF 60 Sunny Face
Product NDC 79950-019
11-digit product format 799500019
Labeler code 79950
Product ID 79950-019_24c78897-3137-f24b-e063-6394a90aa80a
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form LOTION
Route TOPICAL
Labeler BONDI SANDS (USA) INC.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-08
Substance AVOBENZONE; OCTISALATE; OCTOCRYLENE; HOMOSALATE
Active strength 30; 50; 100; 150 mg/mL; mg/mL; mg/mL; mg/mL
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 Bondi Sands SPF 60 Sunny Face
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 100 mg/mL HOMOSALATE 150 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79950-019-01 Bondi Sands SPF 60 Sunny Face 50 mL in 1 TUBE LOTION 50 1 79950-019-01 Bondi Sands SPF 60 Sunny Face 1 in 1 CARTON LOTION 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79950-019 BONDI SANDS SPF 60 SUNNY FACE (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BONDI SANDS (USA) INC.] 1 Current NDC, 2 package rows 20250112_24c78897-3136-f24b-e063-6394a90aa80a.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 Sample Exclude flag Status 79950-019-01 79950001901 1 TUBE in 1 CARTON (79950-019-01) / 50 mL in 1 TUBE 1 tube 2025-01-08 No No Current