Home NDC 0132-0324 Boudreauxs
Product NDC 0132-0324
11-digit product format 001320324
Labeler code 0132
Product ID 0132-0324_d9877348-ea83-416f-90b9-8862ec408afe
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form OINTMENT
Route TOPICAL
Labeler C.B. Fleet Company, Inc.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-12-02
Substance ZINC OXIDE
Active strength 16 g/113g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2027-12-31
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 · 8 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…
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 Boudreauxs
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 16 g/113g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 708071 Internal RxNorm 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 0132-0324-02 Boudreauxs 1 in 1 CARTON OINTMENT 1 5 0132-0324-02 Boudreauxs 57 g in 1 TUBE OINTMENT 57 5 0132-0324-04 Boudreauxs 1 in 1 CARTON OINTMENT 1 5 0132-0324-04 Boudreauxs 113 g in 1 TUBE OINTMENT 113 5 0132-0324-14 Boudreauxs 396 g in 1 JAR OINTMENT 396 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0132-0324 BOUDREAUXS (ZINC OXIDE) OINTMENT [C.B. FLEET COMPANY, INC.] 4 Current NDC, Legacy NDC, 5 package rows 20250116_f8f626c8-13ae-4b3b-ae3f-e0dc800fcb4a.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 55 of 68 · 1,357 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0132-0324-02 00132032402 1 TUBE in 1 CARTON (0132-0324-02) > 57 g in 1 TUBE 1 tube 2019-12-02 0000-00-00 No No Current 0132-0324-04 00132032404 1 TUBE in 1 CARTON (0132-0324-04) / 113 g in 1 TUBE 1 tube 2019-12-02 0000-00-00 No No Current 0132-0324-14 00132032414 396 g in 1 JAR (0132-0324-14) 396 g 2019-12-02 0000-00-00 No No Current