Home NDC 72288-180 Petrolatum
Product NDC 72288-180
11-digit product format 722880180
Labeler code 72288
Product ID 72288-180_5cc92f0c-18ed-af78-e063-6394a90a559d
Type HUMAN OTC DRUG
Nonproprietary name Petrolatum
Dosage form OINTMENT
Route TOPICAL
Labeler Amazon.com Services LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-04-25
Substance PETROLATUM
Active strength 410 mg/g
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 · 6 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…
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 Petrolatum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PETROLATUM 410 mg/g
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72288-180-17 Petrolatum 50 g in 1 TUBE OINTMENT 50 21 72288-180-41 Petrolatum 396 g in 1 JAR OINTMENT 396 21
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72288-180 PETROLATUM OINTMENT [AMAZON.COM SERVICES LLC] 19 Current NDC, Legacy NDC, 2 package rows 20250221_833b5af7-8db1-4f88-bf4d-9cf32c7cf795.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 30 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 72288-180-17 72288018017 50 g in 1 TUBE (72288-180-17) 50 g 2018-04-25 0000-00-00 No No Current 72288-180-41 72288018041 396 g in 1 JAR (72288-180-41) 396 g 2018-04-25 0000-00-00 No No Current