Home NDC 61957-3701 Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 0N Neutral
Product NDC 61957-3701
11-digit product format 619573701
Labeler code 61957
Product ID 61957-3701_50ae9e7b-7bec-d90a-e063-6394a90a214a
Type HUMAN OTC DRUG
Nonproprietary name OCTISALATE, TITANIUM DIOXIDE
Dosage form EMULSION
Route TOPICAL
Labeler Parfums Christian Dior
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-09-01
Substance OCTISALATE; TITANIUM DIOXIDE
Active strength 51; 48 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 Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 0N Neutral
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 51 mg/mL TITANIUM DIOXIDE 48 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup 15FIX9V2JP 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 Units Marketing start Sample Exclude flag Status 61957-3701-0 61957370100 1 BOTTLE in 1 CARTON (61957-3701-0) / 40 mL in 1 BOTTLE 1 bottle 2026-09-01 No No Current