Home NDC 78863-1012 Brush and Go
Product NDC 78863-1012
11-digit product format 788631012
Labeler code 78863
Product ID 78863-1012_62095164-22c2-48fe-8160-4a10b94b0156
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, and Oxybenzone
Dosage form POWDER
Route TOPICAL
Labeler Noon Aesthetics M.R. Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-05-01
Substance TITANIUM DIOXIDE; OCTINOXATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE; OXYBENZONE
Active strength 1.25; .236; .225; .135; .075; .075 g/5g; g/5g; g/5g; g/5g; g/5g; g/5g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 78863-1012-2 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 78863-1012-2 0efc9e666f02…f202fb6c5f17…
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 Brush and Go
Brand name suffix Oily Problematic Skin
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 1.25 g/5g OCTINOXATE .236 g/5g OCTOCRYLENE .225 g/5g OCTISALATE .135 g/5g AVOBENZONE .075 g/5g OXYBENZONE .075 g/5g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
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 78863-1012-2 Brush and Go Oily Problematic Skin 5 g in 1 BOTTLE, WITH APPLICATOR POWDER 5 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 78863-1012 BRUSH AND GO OILY PROBLEMATIC SKIN (TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE) POWDER BRUSH AND GO OILY PROBLEMATIC SKIN MATTE FINISH TONE 1 (TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE) POWDER BRUSH AND GO OILY PROBLEMATIC SKIN MATTE FINISH TONE 2 (TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE) POWDER [NOON AESTHETICS M.R. LTD] 5 Current NDC, Legacy NDC, 1 package rows 20250130_b4295453-f193-4bed-be5b-efcd91772107.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 109 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 78863-1012-2 78863101202 5 g in 1 BOTTLE, WITH APPLICATOR (78863-1012-2) 5 g 2020-05-01 0000-00-00 No No Current