Home NDC 98132-159-03 BareMinerals
Product NDC 98132-159
Requested package NDC 98132-159-03
11-digit product format 981320159
Labeler code 98132
Product ID 98132-159_06e82259-5f4c-e44a-e063-6394a90a45ce
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide and Zinc Oxide
Dosage form POWDER
Route TOPICAL
Labeler Orveon Global US LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2009-07-30
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 25; 10 g/100g; g/100g
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 · 7 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
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 BareMinerals
Brand name suffix Mineral Veil
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 25 g/100g ZINC OXIDE 10 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 98132-159-02 BareMineralsMineral Veil 1.5 g in 1 JAR POWDER 1.5 4 98132-159-03 BareMineralsMineral Veil 6 g in 1 JAR POWDER 6 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 98132-159 BAREMINERALS MINERAL VEIL (TITANIUM DIOXIDE AND ZINC OXIDE) POWDER BAREMINERALS TINTED MINERAL VEIL (TITANIUM DIOXIDE AND ZINC OXIDE) POWDER [ORVEON GLOBAL US LLC] 4 Current NDC, Legacy NDC, 2 package rows 20231214_64b163dd-8a86-483f-8dab-80fa8740b12f.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 Marketing end Sample Exclude flag Status 98132-159-03 98132015903 6 g in 1 JAR (98132-159-03) 6 g 2009-07-30 0000-00-00 No No Current