FDA.reportPublic FDA data

SPOT CARE GREEN ONE

Manufacturer
Leejiham
Effective date
2020-09-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:15:30

Label at a glance#

ProductSPOT CARE GREEN ONE
Active ingredientBENZYL ALCOHOL, ALCOHOL
Label structure11 sections

Indications and uses

Water type ampule for calming skin irritation and blemish-prone skin and even relieving acne skin.

Dosage and administration

Soak cotton pad and apply over the face except eye and lip areas after using Blue One.

Storage and handling

Protect this product from direct sun and excessive heat

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 2%

Glycerin 0.01%

Benzyl Alcohol 0.05%

Purpose

OTC - PURPOSE SECTION

​Skin Protectant

Uses

DOSAGE & ADMINISTRATION SECTION

Water type ampule for calming skin irritation and blemish-prone skin and even relieving acne skin.

Directions

INDICATIONS & USAGE SECTION

Soak cotton pad and apply over the face except eye and lip areas after using Blue One.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Alcohol, Sodium PCA, Butylene Glycol, Sodium Lactate, Dipotassium Glycyrrhizate, Methyl Gluceth-20, Potassium Chloride, Pinus Sylvestris Leaf Extract, Pentylene Glycol, Caprylyl Glycol, Arginine, Betaine, Ethylhexylglycerin, Sorbitol, Sodium Hyaluronate, Portulaca Oleracea Extract, Glycine, Glutamic Acid, Alanine, Lysine, Threonine, Proline, Glycyrrhiza Uralensis (Licorice) Root Extract, Silkworm Extract, Morus Alba Bark Extract, Opuntia Coccinellifera Fruit Extract, Diospyros Kaki Leaf Extract, Rehmannia Glutinosa Root Extract, Cornus Officinalis Fruit Extract, Dioscorea Japonica Root Extract, Alisma Orientale Tuber Extract, Poria Cocos Sclerotium Extract,Paeonia Suffruticosa Root Extract, Chamomilla Recutita (Matricaria) Flower Water, Artemisia Princeps Leaf Extract, Benzyl Alcohol, Chlorphenesin

Warnings

WARNINGS SECTION

For external use only

Stop use and ask a physician

OTC - ASK DOCTOR SECTION

if skin irritation and redness occurs more than 72 hours.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help right away.

Other information

STORAGE AND HANDLING SECTION

Protect this product from direct sun and excessive heat

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30ml NDC: 80395-204-01 Label 130ml NDC: 80395-204-01 Label 1

30ml NDC: 80395-204-01 Label 230ml NDC: 80395-204-01 Label 2

50ml NDC: 80395-204-02 Label50ml NDC: 80395-204-02 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80395-204-012022-06-14C16284748780-1d6a99b39-476f-a426-e053-dadaa90af4c280395-204
80395-204-022022-06-14C16284748780-1d6a99b39-476f-a426-e053-dadaa90af4c280395-204
80395-204-012022-01-28C16284748780-1d6a99b39-476f-a426-e053-dadaa90af4c280395-204
80395-204-022022-01-28C16284748780-1d6a99b39-476f-a426-e053-dadaa90af4c280395-204

Products#

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

DailyMed product names page 1 of 2 · 43 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80395-20480395-204-01, 80395-204-02

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 41 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARTEMISIA PRINCEPS LEAFSY077EW02GIACT
CHLORPHENESINI670DAL4SZIACT
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
SODIUM LACTATETU7HW0W0QTIACT
METHYL GLUCETH-20J3QD0LD11PIACT
PINE NEEDLE OIL (PINUS SYLVESTRIS)5EXL5H740YIACT
PENTYLENE GLYCOL50C1307PZGIACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLUTAMIC ACID3KX376GY7LIACT
SORBITOL506T60A25RIACT
SERINE452VLY9402IACT
GLYCINETE7660XO1CIACT
ALANINEOF5P57N2ZXIACT
LYSINEK3Z4F929H6IACT
BENZYL ALCOHOLLKG8494WBHACTIB
BETAINE3SCV180C9WIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ALCOHOL3K9958V90MACTIB
SODIUM PYRROLIDONE CARBOXYLATE469OTG57A2IACT
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXIACT
POTASSIUM CHLORIDE660YQ98I10IACT
ARGININE94ZLA3W45FIACT
HYALURONATE SODIUMYSE9PPT4THIACT
PURSLANEM6S840WXG5IACT
PROLINE9DLQ4CIU6VIACT
GLYCYRRHIZA URALENSIS ROOT42B5YD8F0KIACT
BOMBYX MORI LARVA1WYM0QWX33IACT
MORUS ALBA BARK7O71A48NDPIACT
OPUNTIA COCHENILLIFERA FRUIT838ZTK02KHIACT
DIOSPYROS KAKI LEAFQ71GF9OBNOIACT
REHMANNIA GLUTINOSA ROOT1BEM3U6LQQIACT
CORNUS OFFICINALIS FRUIT23NL8NQ187IACT
ALISMA PLANTAGO-AQUATICA SUBSP. ORIENTALE ROOT555C7I140LIACT
PAEONIA X SUFFRUTICOSA ROOT7M7E9A2C8JIACT
THREONINE2ZD004190SIACT
DIOSCOREA JAPONICA ROOTI43FCF3356IACT
FU LINGXH37TWY5O4IACT
CHAMOMILE FLOWER OIL60F80Z61A9IACT
ASIAN GINSENGCUQ3A77YXIIACT

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
e173c1a3-69eb-9374-e053-2a95a90a4b84ae510c7f-f209-6bea-e053-2995a90a90d12022-06-14WarningsExact identifier
spl set id: ae510c7f-f209-6bea-e053-2995a90a90d1

Reported adverse events (FAERS/openFDA)#

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