Home NDC 42893-101 Chantecaille Ultra Sun Protection Sunscreen SPF 45
Product NDC 42893-101
11-digit product format 428930101
Labeler code 42893
Product ID 42893-101_5a7f7a85-8432-2cff-e063-6394a90ac4d7
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE
Dosage form LIQUID
Route TOPICAL
Labeler Chantecaille Beaute Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-01
Substance AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 74.9; 50; 27.5 mg/mL; mg/mL; mg/mL; mg/mL
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 Chantecaille Ultra Sun Protection Sunscreen SPF 45
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL OCTINOXATE 74.9 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 27.5 mg/mL
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.
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 128 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 42893-101-00 42893010100 1 TUBE in 1 CARTON (42893-101-00) / 40 mL in 1 TUBE 1 tube 2026-05-01 No No Current