FDA.reportPublic FDA data

LAVENDER HAND SANITIZER

Manufacturer
THURINGEN KOREA Co., Ltd.
Effective date
2020-12-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:36

Label at a glance#

ProductLAVENDER HAND SANITIZER
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100100

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN1
1041849ethanol 0.7 ML/ML Topical SpraySCD1
1041849ethanol 70 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74864-0001-12022-01-28C16284748780-1d6a99b39-4bc5-a426-e053-dadaa90af4c2Lavender Hand Sanitizer Spary: 74864-0001
74864-0001-22022-01-28C16284748780-1d6a99b39-4bc5-a426-e053-dadaa90af4c2Lavender Hand Sanitizer Spary: 74864-0001
74864-0001-32022-01-28C16284748780-1d6a99b39-4bc5-a426-e053-dadaa90af4c2Lavender Hand Sanitizer Spary: 74864-0001

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74864-0001-1LAVENDER HAND SANITIZER100 mL in 1 BOTTLE, SPRAYSPRAY1001
74864-0001-2LAVENDER HAND SANITIZER250 mL in 1 BOTTLE, SPRAYSPRAY2501
74864-0001-3LAVENDER HAND SANITIZER500 mL in 1 BOTTLE, SPRAYSPRAY5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74864-0001LAVENDER HAND SANITIZER (ALCOHOL) SPRAY [THURINGEN KOREA CO., LTD.]1Legacy NDC, 3 package rows20201204_5ea1ef2e-7bbb-4516-8c6f-e35f2996738a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74864-000174864-0001-1, 74864-0001-2, 74864-0001-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TEA TREE OILVIF565UC2GIACT
LAVENDER OILZBP1YXW0H8IACT
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 806OZP39ZG8HIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b598a86f-0f66-6af2-e053-2995a90aab7d5ea1ef2e-7bbb-4516-8c6f-e35f2996738a2020-12-03Exact identifier
spl id: b598a86f-0f66-6af2-e053-2995a90aab7d
spl set id: 5ea1ef2e-7bbb-4516-8c6f-e35f2996738a

Reported adverse events (FAERS/openFDA)#

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