Home NDC 79903-007 Tanning Sunscreen UVB Protection Dry Oil
Product NDC 79903-007
11-digit product format 799030007
Labeler code 79903
Product ID 79903-007_25288480-1e92-9afb-e063-6294a90a32c3
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler WAL-MART STORES INC.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-08-31
Substance HOMOSALATE; OCTISALATE; AVOBENZONE
Active strength 100; 50; 20 mg/g; mg/g; mg/g
NDC exclude flag No
Listing certified through 2027-12-31
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 Tanning Sunscreen UVB Protection Dry Oil
Brand name suffix Equate
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/g OCTISALATE 50 mg/g AVOBENZONE 20 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V06SV4M95S Internal UNII lookup 4X49Y0596W Internal UNII lookup G63QQF2NOX 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 79903-007-37 Tanning Sunscreen UVB Protection Dry OilEquate 156 g in 1 CAN AEROSOL, SPRAY 156 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79903-007 TANNING SUNSCREEN UVB PROTECTION DRY OIL EQUATE (AVOBENZONE, HOMOSALATE, OCTISALATE) AEROSOL, SPRAY [WAL-MART STORES INC.] 3 Current NDC, Legacy NDC, 1 package rows 20241025_acdf62f2-742e-5df9-e053-2a95a90a96c5.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 Marketing end Sample Exclude flag Status 79903-007-37 79903000737 156 g in 1 CAN (79903-007-37) 156 g 2020-08-31 0000-00-00 No No Current