Home NDC 72839-543 SPF 50 Sunscreen
Product NDC 72839-543
11-digit product format 728390543
Labeler code 72839
Product ID 72839-543_29a617df-d38b-dcbc-e063-6394a90a43f2
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%
Dosage form SPRAY
Route TOPICAL
Labeler Derma Care Research Labs, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-03-27
Substance OCTISALATE; AVOBENZONE; HOMOSALATE; OCTOCRYLENE
Active strength 5; 3; 15; 10 g/100mL; g/100mL; g/100mL; g/100mL
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 SPF 50 Sunscreen
Brand name suffix Rocky Mountain
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 5 g/100mL AVOBENZONE 3 g/100mL HOMOSALATE 15 g/100mL OCTOCRYLENE 10 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 72839-543-06 SPF 50 SunscreenRocky Mountain 177 mL in 1 CAN SPRAY 177 3 72839-543-16 SPF 50 SunscreenRocky Mountain 473 mL in 1 BOTTLE, PUMP SPRAY 473 3 72839-543-32 SPF 50 SunscreenRocky Mountain 946 mL in 1 BOTTLE, PUMP SPRAY 946 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72839-543 SPF 50 SUNSCREEN ROCKY MOUNTAIN (AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%) SPRAY [DERMA CARE RESEARCH LABS, LLC] 3 Current NDC, Legacy NDC, 3 package rows 20241222_a1c9066c-4801-5aee-e053-2995a90a75d2.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 27 of 354 · 7,077 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 72839-543-06 72839054306 177 mL in 1 CAN (72839-543-06) 177 ml 2020-03-27 0000-00-00 No No Current 72839-543-16 72839054316 473 mL in 1 BOTTLE, PUMP (72839-543-16) 473 ml 2020-03-27 0000-00-00 No No Current 72839-543-32 72839054332 946 mL in 1 BOTTLE, PUMP (72839-543-32) 946 ml 2020-03-27 0000-00-00 No No Current