Bondi Sands Sport SPF 50 Sunscreen

Product NDC
79950-010
Requested package NDC
79950-010-01
11-digit product format
799500010
Labeler code
79950
Product ID
79950-010_c31445d3-a745-f7d6-e053-2a95a90a52b6
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
BONDI SANDS (USA) INC.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-05-24
Marketing end
0000-00-00
Substance
AVOBENZONE; OCTISALATE; OCTOCRYLENE; HOMOSALATE
Active strength
18 mg/g; mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage79950-01079950-010-01IInactivated by FDA2026-08-07

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79950-010-01Bondi Sands Sport SPF 50 Sunscreen160 g in 1 CANAEROSOL, SPRAY1602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79950-010BONDI SANDS SPORT SPF 50 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) AEROSOL, SPRAY [BONDI SANDS (USA) INC.]2Legacy NDC, 1 package rows20241108_c3143b7a-e6bd-5b24-e053-2995a90aef2d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79950-010-0179950001001160 g in 1 CAN (79950-010-01) 160 g2021-05-240000-00-00NoNoCurrent