Home NDC 78261-324 Natural Sense SPF 50 Sunscreen
Product NDC 78261-324
11-digit product format 782610324
Labeler code 78261
Product ID 78261-324_51dab08e-6412-eb67-e063-6294a90a520c
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen
Dosage form CLOTH
Route TOPICAL
Labeler Dr. Natural LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-01
Substance OCTINOXATE; AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength 5; 3; 3; 6 g/100g; g/100g; g/100g; g/100g
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 Natural Sense SPF 50 Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 5 g/100g AVOBENZONE 3 g/100g OCTISALATE 3 g/100g OCTOCRYLENE 6 g/100g
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 78261-324-09 Natural Sense SPF 50 Sunscreen 25 g in 1 PACKET CLOTH 25 2
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 Sample Exclude flag Status 78261-324-09 78261032409 25 g in 1 PACKET (78261-324-09) 25 g 2026-01-01 No No Current