Home NDC 71070-599 Jacket Ultimate Performance Sunscreen SPF 30
Product NDC 71070-599
11-digit product format 710700599
Labeler code 71070
Product ID 71070-599_3462c3ff-351f-de3c-e063-6394a90a947c
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, OCTISALATE, OCTOCRYLENE
Dosage form LIQUID
Route TOPICAL
Labeler BALSHI MD DERMACEUTICALS
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-08
Substance AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength 30; 50; 50 mg/mL; mg/mL; mg/mL
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 Jacket Ultimate Performance Sunscreen SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup 4X49Y0596W Internal UNII lookup 5A68WGF6WM 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 71070-599-00 Jacket Ultimate Performance Sunscreen SPF 30 177 mL in 1 CAN LIQUID 177 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71070-599 JACKET ULTIMATE PERFORMANCE SUNSCREEN SPF 30 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) LIQUID [BALSHI MD DERMACEUTICALS] 1 Current NDC, 1 package rows 20250507_d4d82c41-01da-40af-a22c-d4d57af7a2f2.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 45 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 71070-599-00 71070059900 177 mL in 1 CAN (71070-599-00) 177 ml 2025-04-08 No No Current