Home NDC 64141-034-01 WEIGHTLESS SKIN FOUNDATION BROAD SPECTRUM SPF 15
Product NDC 64141-034
Requested package NDC 64141-034-01
11-digit product format 641410034
Labeler code 64141
Product ID 64141-034_29238e5b-eff5-e729-e063-6394a90aec64
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, TITANIUM DIOXIDE
Dosage form EMULSION
Route TOPICAL
Labeler Bobbi Brown Professional Cosmetics Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-05-16
Substance OCTINOXATE; TITANIUM DIOXIDE
Active strength 67; 17 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 WEIGHTLESS SKIN FOUNDATION BROAD SPECTRUM SPF 15
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 67 mg/mL TITANIUM DIOXIDE 17 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 15FIX9V2JP 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 64141-034-01 WEIGHTLESS SKIN FOUNDATION BROAD SPECTRUM SPF 15 30 mL in 1 BOTTLE EMULSION 30 2 64141-034-01 WEIGHTLESS SKIN FOUNDATION BROAD SPECTRUM SPF 15 1 in 1 CARTON EMULSION 1 2 64141-034-02 WEIGHTLESS SKIN FOUNDATION BROAD SPECTRUM SPF 15 13 mL in 1 BOTTLE EMULSION 13 2 64141-034-02 WEIGHTLESS SKIN FOUNDATION BROAD SPECTRUM SPF 15 1 in 1 CARTON EMULSION 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64141-034 WEIGHTLESS SKIN FOUNDATION BROAD SPECTRUM SPF 15 (OCTINOXATE, TITANIUM DIOXIDE) EMULSION [BOBBI BROWN PROFESSIONAL COSMETICS INC.] 2 Current NDC, 4 package rows 20241215_fbd04b66-738b-2762-e053-6394a90a8b72.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 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 64141-034-01 64141003401 1 BOTTLE in 1 CARTON (64141-034-01) / 30 mL in 1 BOTTLE 1 bottle 2023-05-16 No No Current