SAFERENCE SANITIZER

Manufacturer
MAY MEDIC CO LTD
Effective date
2020-04-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:52

Label at a glance#

ProductSAFERENCE SANITIZER
Active ingredientLAVENDER OIL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

lavender oil

OTC - PURPOSE SECTION

see attached Drug Facts label

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

WARNINGS SECTION

see attached Drug Facts label

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

silia, water, propanediol, olive oil, etc (see attached Drug Facts label)

INDICATIONS & USAGE SECTION

pour small amount into hands, spread evenly and rub into the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
75693-0001-12022-01-28C16284748780-1d6a99b39-d74f-a426-e053-dadaa90af4c2Drug Facts
75693-0001-22022-01-28C16284748780-1d6a99b39-d74f-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75693-0001-1SAFERENCE SANITIZER500 mL in 1 BOTTLELIQUID5001
75693-0001-2SAFERENCE SANITIZER50 mL in 1 BOTTLELIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75693-0001SAFERENCE SANITIZER (LAVANDULA ANGUSTIFOLIA OIL) LIQUID [MAY MEDIC CO LTD]1Legacy NDC, 2 package rows20200425_a40aeebf-5675-54b1-e053-2995a90a5093.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75693-000175693-0001-1, 75693-0001-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
a40aeebf-5676-54b1-e053-2995a90a5093a40aeebf-5675-54b1-e053-2995a90a50932020-04-24WarningsExact identifier
spl id: a40aeebf-5676-54b1-e053-2995a90a5093
spl set id: a40aeebf-5675-54b1-e053-2995a90a5093

Reported adverse events (FAERS/openFDA)#

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