Bondi Sands Fragrance Free SPF 50 Sunscreen

Product NDC
79950-005
11-digit product format
799500005
Labeler code
79950
Product ID
79950-005_26435275-982b-2b05-e063-6294a90a3034
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
2021-01-01
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 50; 80 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 Fragrance Free SPF 50 Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE80 mg/mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79950-005-01Bondi Sands Fragrance Free SPF 50 Sunscreen150 mL in 1 TUBELOTION1502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79950-005BONDI SANDS FRAGRANCE FREE SPF 50 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BONDI SANDS (USA) INC.]2Current NDC, Legacy NDC, 1 package rows20241108_acda604c-27cf-d500-e053-2995a90a5d65.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79950-005-0179950000501150 mL in 1 TUBE (79950-005-01) 150 ml2021-01-010000-00-00NoNoCurrent