FDA.reportPublic FDA data

Lavaderm After Sun

Product NDC
70631-034
Requested package NDC
70631-034-25
11-digit product format
706310034
Labeler code
70631
Product ID
70631-034_f1d6d188-81a7-54c0-e053-2995a90a8f1f
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
SPRAY
Route
TOPICAL
Labeler
Young Living Essential Oils, LC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-04-05
Marketing end
0000-00-00
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
0 g/g
NDC exclude flag
No
Listing certified through
2024-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage70631-03470631-034-25IInactivated by FDA2026-10-05

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 · 4 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2024-07-10 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.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70631-034-252024-09-16C16284748780-10191ceaa-6be1-198a-e063-dbdaa90aec3eLavaderm After Sun
70631-034-252023-07-28C16284748780-10191ceaa-6be1-198a-e063-dbdaa90aec3eLavaderm After Sun

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70631-034-25Lavaderm After SunFor Pain and Itching1 in 1 BOXSPRAY14
70631-034-25Lavaderm After SunFor Pain and Itching57 g in 1 BOTTLE, SPRAYSPRAY574

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70631-034LAVADERM AFTER SUN FOR PAIN AND ITCHING (MENTHOL) SPRAY [YOUNG LIVING ESSENTIAL OILS, LC]4Legacy NDC, 2 package rows20240918_4c6e4fd7-3306-2936-e054-00144ff8d46c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1314935menthol 0.5 % Topical SprayPSN4c6e4fd7-3306-2936-e054-00144ff8d46c4
1314935menthol 5 MG/ML Topical SpraySCD4c6e4fd7-3306-2936-e054-00144ff8d46c4
1314935menthol 0.5 % Topical SpraySY4c6e4fd7-3306-2936-e054-00144ff8d46c4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70631-034-25706310034251 BOTTLE, SPRAY in 1 BOX (70631-034-25) > 57 g in 1 BOTTLE, SPRAY2017-04-050000-00-00NoNoCurrent