Home NDC 87416-002 Acewink Sunscreen
Product NDC 87416-002
11-digit product format 874160002
Labeler code 87416
Product ID 87416-002_53d19fa8-6f0f-2c11-e063-6294a90abb03
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen Spray
Dosage form SPRAY
Route TOPICAL
Labeler Shenzhen Qiming Biotechnology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-10
Substance OCTOCRYLENE; OCTISALATE; OCTINOXATE
Active strength 2; 4; 7.5 mg/100mg; mg/100mg; mg/100mg
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 Acewink Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 2 mg/100mg OCTISALATE 4 mg/100mg OCTINOXATE 7.5 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5A68WGF6WM Internal UNII lookup 4X49Y0596W Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 Marketing start Sample Exclude flag Status 87416-002-02 87416000202 1 BOTTLE, SPRAY in 1 BOX (87416-002-02) / 1 mg in 1 BOTTLE, SPRAY (87416-002-01) 2026-06-10 No No Current