Home NDC 52000-005-25 UNIVERSAL PURE PETROLEUM
Product NDC 52000-005
Requested package NDC 52000-005-25
11-digit product format 520000005
Labeler code 52000
Product ID 52000-005_450aaf36-540f-c00f-e063-6394a90a6edf
Type HUMAN OTC DRUG
Nonproprietary name White Petroleum
Dosage form JELLY
Route TOPICAL
Labeler Universal Distribution Center LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-02-06
Substance PETROLATUM
Active strength 1 g/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 2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 9bebd1f3094a…5416666fcb17…
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 UNIVERSAL PURE PETROLEUM
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PETROLATUM 1 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4T6H12BN9U Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 204754 Internal RxNorm 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 52000-005-19 UNIVERSAL PURE PETROLEUM 226 g in 1 JAR JELLY 226 6 52000-005-20 UNIVERSAL PURE PETROLEUM 45 g in 1 JAR JELLY 45 6 52000-005-21 UNIVERSAL PURE PETROLEUM 100 g in 1 JAR JELLY 100 6 52000-005-22 UNIVERSAL PURE PETROLEUM 113 g in 1 JAR JELLY 113 6 52000-005-23 UNIVERSAL PURE PETROLEUM 170 g in 1 JAR JELLY 170 6 52000-005-24 UNIVERSAL PURE PETROLEUM 198 g in 1 JAR JELLY 198 6 52000-005-25 UNIVERSAL PURE PETROLEUM 283 g in 1 JAR JELLY 283 6 52000-005-26 UNIVERSAL PURE PETROLEUM 368 g in 1 JAR JELLY 368 6 52000-005-27 UNIVERSAL PURE PETROLEUM 450 g in 1 JAR JELLY 450 6 52000-005-28 UNIVERSAL PURE PETROLEUM 500 g in 1 JAR JELLY 500 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52000-005 UNIVERSAL PURE PETROLEUM (WHITE PETROLEUM) JELLY [UNIVERSAL DISTRIBUTION CENTER LLC] 5 Current NDC, Legacy NDC, 10 package rows 20241212_6bc34bbe-e324-48f4-b6df-dd508b19c2e2.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 6 of 68 · 1,350 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 52000-005-25 52000000525 283 g in 1 JAR (52000-005-25) 283 g 2022-11-07 0000-00-00 No No Current