Home NDC 42213-360-28 ULTRA SEAL Triple Antibiotic
Product NDC 42213-360
Requested package NDC 42213-360-28
11-digit product format 422130360
Labeler code 42213
Product ID 42213-360_9626a7c9-b05f-b11d-e053-2a95a90a7707
Type HUMAN OTC DRUG
Nonproprietary name neomycin, polymixin, bacitracin
Dosage form OINTMENT
Route TOPICAL
Labeler Ultra Seal Corporation
Application part333B
Marketing category OTC MONOGRAPH FINAL
Marketing start 2011-04-12
Marketing end 0000-00-00
Substance NEOMYCIN SULFATE; POLYMYXIN B SULFATE; BACITRACIN ZINC
Active strength 5 mg/g; [iU]/g; [iU]/g
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record 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 · 12 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…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BACITRACIN ZINC ACTIVE INGREDIENT 89Y4M234ES ULTRA SEAL TRIPLE ANTIBIOTIC (NEOMYCIN, POLYMIXIN, BACITRACIN) OINTMENT [ULTRA SEAL CORPORATION] 1 NEOMYCIN SULFATE ACTIVE INGREDIENT 057Y626693 ULTRA SEAL TRIPLE ANTIBIOTIC (NEOMYCIN, POLYMIXIN, BACITRACIN) OINTMENT [ULTRA SEAL CORPORATION] 1 POLYMYXIN B SULFATE ACTIVE INGREDIENT 19371312D4 ULTRA SEAL TRIPLE ANTIBIOTIC (NEOMYCIN, POLYMIXIN, BACITRACIN) OINTMENT [ULTRA SEAL CORPORATION] 1 BACITRACIN ACTIVE MOIETY 58H6RWO52I ULTRA SEAL TRIPLE ANTIBIOTIC (NEOMYCIN, POLYMIXIN, BACITRACIN) OINTMENT [ULTRA SEAL CORPORATION] 1 NEOMYCIN ACTIVE MOIETY I16QD7X297 ULTRA SEAL TRIPLE ANTIBIOTIC (NEOMYCIN, POLYMIXIN, BACITRACIN) OINTMENT [ULTRA SEAL CORPORATION] 1 POLYMYXIN B ACTIVE MOIETY J2VZ07J96K ULTRA SEAL TRIPLE ANTIBIOTIC (NEOMYCIN, POLYMIXIN, BACITRACIN) OINTMENT [ULTRA SEAL CORPORATION] 1 PETROLATUM INACTIVE INGREDIENT 4T6H12BN9U ULTRA SEAL TRIPLE ANTIBIOTIC (NEOMYCIN, POLYMIXIN, BACITRACIN) OINTMENT [ULTRA SEAL CORPORATION] 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 42213-360-28 42213036028 1 TUBE in 1 CARTON (42213-360-28) > 28 g in 1 TUBE 1 tube 2019-09-05 0000-00-00 No No Current