FDA.reportPublic FDA data

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; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 150; 50; 100 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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
IngredientStrength
AVOBENZONE30 mg/mL
OCTISALATE150 mg/mL
OCTOCRYLENE50 mg/mL
HOMOSALATE100 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, 4X49Y0596W, 5A68WGF6WM, V06SV4M95S

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79950-019-01Bondi Sands SPF 60 Sunny Face50 mL in 1 TUBELOTION501
79950-019-01Bondi Sands SPF 60 Sunny Face1 in 1 CARTONLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79950-019BONDI SANDS SPF 60 SUNNY FACE (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BONDI SANDS (USA) INC.]1Current NDC, 2 package rows20250112_24c78897-3136-f24b-e063-6394a90aa80a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
79950-019-01799500019011 TUBE in 1 CARTON (79950-019-01) / 50 mL in 1 TUBE1 tube2025-01-08NoNoHistorical