Home NDC 79950-002 Bondi Sands Toasted Coconut Lip Balm with SPF 50 Sunscreen
Product NDC 79950-002
11-digit product format 799500002
Labeler code 79950
Product ID 79950-002_26436451-e1db-ad8f-e063-6394a90a0f38
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octocrylene
Dosage form LIPSTICK
Route TOPICAL
Labeler BONDI SANDS (USA) INC.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-01
Substance AVOBENZONE; OCTOCRYLENE; HOMOSALATE
Active strength 30; 40; 80 mg/g; mg/g; mg/g
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 Toasted Coconut Lip Balm with SPF 50 Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/g OCTOCRYLENE 40 mg/g HOMOSALATE 80 mg/g
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 5A68WGF6WM Internal UNII lookup V06SV4M95S 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 79950-002-01 Bondi Sands Toasted Coconut Lip Balm with SPF 50 Sunscreen 10 g in 1 TUBE, WITH APPLICATOR LIPSTICK 10 3 79950-002-01 Bondi Sands Toasted Coconut Lip Balm with SPF 50 Sunscreen 1 in 1 CARTON LIPSTICK 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79950-002 BONDI SANDS TOASTED COCONUT LIP BALM WITH SPF 50 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTOCRYLENE) LIPSTICK [BONDI SANDS (USA) INC.] 3 Current NDC, Legacy NDC, 2 package rows 20241108_acb8513e-723b-b7d6-e053-2995a90aed52.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 Marketing start Marketing end Sample Exclude flag Status 79950-002-01 79950000201 1 TUBE, WITH APPLICATOR in 1 CARTON (79950-002-01) / 10 g in 1 TUBE, WITH APPLICATOR 2021-01-01 0000-00-00 No No Current