LavaDerm AfterSun

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: LavaDerm AfterSun
Generic name: MENTHOL
Manufacturer: Young Living Essential Oils, LC.
Product type: HUMAN OTC DRUG
SPL set ID: 4fcddcf1-36db-2f1a-e054-00144ff8d46c
SPL ID: 4f8770bb-310d-48d9-e063-6294a90afcdb
Version: 4
Effective date: 2026-04-15
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:36:12

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		LavaDerm AfterSun	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Young Living Essential Oils, LC.	openfda.manufacturer_name
ndc	package	70631-067-57	openfda.package_ndc
ndc	product	70631-067	openfda.product_ndc
ndc11	package	70631006757	derived:openfda.package_ndc
rxcui		1314935	openfda.rxcui
spl id		4f8770bb-310d-48d9-e063-6294a90afcdb	id
spl set id		4fcddcf1-36db-2f1a-e054-00144ff8d46c	set_id
unii		L7T10EIP3A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: For external use only When using this product avoid contact wiith eyes Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children to avoid accidental ingestion. If swallowed, get medical help or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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