FDA.reportPublic FDA data

Alkmene Anti Spot pad

Manufacturer
Mann & Schroeder GmbH
Effective date
2017-01-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:48:35

Label at a glance#

ProductAlkmene Anti Spot pad
Active ingredientTEA TREE OIL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Purpose -

Provides especially gentle care for sensitive and blemished skin.

It's special puricare pimple-fighting ingredient quickly and safely eliminates pimples and blemishes.

The cooling effect of the Alkemene Blemish stick reduces redness and refreshes your complexion.

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT

Tea Tree Oil

DOSAGE & ADMINISTRATION SECTION

Dab onto the affected area and let dry in the morning and evening, or several times a day if needed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach

INACTIVE INGREDIENT SECTION

LINALOOL
ALLANTOIN
GLYCERIN
ASCORBYL PALMITATE
TOCOPHEROL
MANUKA OIL
CARBOMER 934
MAGNOLIA GRANDIFLORA BARK
NIGELLA SATIVA SEED OIL
ACRYLAMIDE
HYDROGENATED PALM GLYCERIDES
AMINO ACIDS
POTASSIUM LAURATE
LECITHIN, SUNFLOWER
PHENOXYETHANOL
BENZYL ALCOHOL
LIMONENE
SODIUM HYDROXIDE
WATER
ALCOHOL

INDICATIONS & USAGE SECTION

Dab onto the affected area and let dry in the morning and evening or serveral times a day.

WARNINGS SECTION

For external use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label 2label 2labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71084-001-012020-01-31C16284748780-19d75b9cf-ece7-f424-e053-dadaa90a57ce463f11de-8bf1-329d-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71084-001-01Alkmene Anti Spot pad15 g in 1 BOTTLELIQUID153

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71084-001ALKMENE ANTI SPOT PAD (GREEN TEA) LIQUID [MANN & SCHROEDER GMBH]3Legacy NDC, 1 package rows20170120_463f11de-8bf1-329d-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71084-00171084-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
ALLANTOIN344S277G0ZIACT
GLYCERINPDC6A3C0OXIACT
ASCORBYL PALMITATEQN83US2B0NIACT
TOCOPHEROLR0ZB2556P8IACT
MANUKA OILM6QU9ZUH2XIACT
CARBOMER 934Z135WT9208IACT
MAGNOLIA GRANDIFLORA BARKJ4XF5T6418IACT
NIGELLA SATIVA SEED OILCS4U38E731IACT
ACRYLAMIDE20R035KLCIIACT
HYDROGENATED PALM GLYCERIDESYCZ8EM144QIACT
TEA TREE OILVIF565UC2GACTIB
POTASSIUM LAURATEV4361R8N4ZIACT
AMINO ACIDS0O72R8RF8AIACT
LECITHIN, SUNFLOWER834K0WOS5GIACT
PHENOXYETHANOLHIE492ZZ3TIACT
.ALPHA.-(.ALPHA.-AMINOPROPYL)BENZYL ALCOHOLS8TT5K3C8YIACT
LIMONENE, (+)-GFD7C86Q1WIACT
SODIUM HYDROXIDE55X04QC32IIACT
LINALOOL, (+/-)-D81QY6I88EIACT

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
46881f19-442b-1afd-e054-00144ff8d46c463f11de-8bf1-329d-e054-00144ff88e882017-01-16WarningsExact identifier
spl id: 46881f19-442b-1afd-e054-00144ff8d46c
spl set id: 463f11de-8bf1-329d-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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