FDA.reportPublic FDA data

Seven Aroma Dr

Manufacturer
Happy Seven Co., Ltd. | ASAN C&S
Effective date
2023-01-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:39:55

Label at a glance#

ProductSeven Aroma Dr
Active ingredientAlcohol
Label structure10 sections

Indications and uses

■ It is used by attaching the solution container to the automatic sprayer.

Dosage and administration

■ wet hands thoroughly with product and allow to dry without wiping ■ supervise children under 6 years of age when using this product to avoid swallowing

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70.0%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ It is used by attaching the solution container to the automatic sprayer.

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

Do not use
• in children less than 2 months of age
• on open skin wounds
When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if
• irritation and redness develop
• condition persists for more than 72hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ wet hands thoroughly with product and allow to dry without wiping
■ supervise children under 6 years of age when using this product to avoid swallowing

Other Information

OTHER SAFETY INFORMATION

■ store between 1-30°C (33.8-86°F)
■ avoid freezing and excessive heat above 40°C (104°F)
■ may discolor certain fabrics or surfaces

Questions

OTC - QUESTIONS SECTION

■ +82-050-672-9002

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Pinus Palustris Twig/Leaf Extract, Camellia Sinensis Leaf Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83225-100-012025-04-30C16284748780-12cef2736-6d96-d83d-e063-dadaa90ab31ff880a2d9-e56d-4d6b-87ed-c985e1e16902
83225-100-012025-01-30C16284748780-12cef2736-6d96-d83d-e063-dadaa90ab31ff880a2d9-e56d-4d6b-87ed-c985e1e16902

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83225-10083225-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT
GREEN TEA LEAFW2ZU1RY8B0IACT

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
33fa075f-8d87-6a0d-e063-6394a90ada3ff880a2d9-e56d-4d6b-87ed-c985e1e169022025-04-30WarningsExact identifier
spl set id: f880a2d9-e56d-4d6b-87ed-c985e1e16902

Reported adverse events (FAERS/openFDA)#

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