skin protectant

Product NDC
64092-254
Requested package NDC
64092-254-04
11-digit product format
640920254
Labeler code
64092
Product ID
64092-254_3b4bf826-51e8-4d71-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
petrolatum
Dosage form
LOTION
Route
TOPICAL
Labeler
Great Lakes Wholesale Marketing and Sales, Inc
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2016-06-30
Marketing end
0000-00-00
Substance
PETROLATUM
Active strength
40 g/133mL
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 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64092-254-042023-01-30C16284748780-1f386c649-c3f6-0266-e053-dadaa90a7c1a395a97cb-45f0-0757-e054-00144ff8d46c

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
64092-254-0464092025404133 mL in 1 TUBE (64092-254-04) 133 ml2016-06-300000-00-00NoNoCurrent