SPOT CARE BLUE 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 BLUE ONE
Active ingredientLACTIC ACID, GLYCERIN, ALCOHOL, BENZYL ALCOHOL, SALICYLIC ACID
Label structure11 sections

Indications and uses

Water type ampule for acne skin caused by excessive sebum and dead skin cells clogging pores.

Dosage and administration

After cleansing, soak cotton butt or cotton pad and apply on acnes.

Storage and handling

Protect this product from direct sun and excessive heat

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80%

Lactic Acid 0.9%

Salicylic Acid 0.45%

Glycerin 0.02%

Benzyl Alcohol 0.1%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Acne

Uses

DOSAGE & ADMINISTRATION SECTION

Water type ampule for acne skin caused by excessive sebum and dead skin cells clogging pores.

Directions

INDICATIONS & USAGE SECTION

After cleansing, soak cotton butt or cotton pad and apply on acnes.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Water, Lactic Acid, Candida Bombicola/Glucose/Methyl Rapeseedate Ferment, Salicylic Acid, Phytosphingosine, Glycerin, Panthenol, Hydrogenated Lecithin, Niacinamide, Raffinose, Ceramide NP, Cholesterol, Hydrogenated Starch Hydrolysate, Glycosyl Trehalose, Ethylhexylglycerin, Silkworm Extract, Scutellaria Baicalensis Root Extract, Illicium Verum (Anise) Fruit Extract, 1,2-Hexanediol, PEG-60 Almond Glycerides, Caprylyl Glycol, Carbomer, Butylene Glycol, Nordihydroguaiaretic Acid, Oleanolic Acid, Benzyl Alcohol

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: 80395-203-01 Label 130ml NDC: 80395-203-01 Label 1

30ml NDC: 80395-203-01 Label 230ml NDC: 80395-203-01 Label 2

50ml NDC: 80395-203-02 Label50ml NDC: 80395-203-02 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80395-203-012022-06-14C16284748780-1d6a99b39-9575-a426-e053-dadaa90af4c280395-203
80395-203-022022-06-14C16284748780-1d6a99b39-9575-a426-e053-dadaa90af4c280395-203
80395-203-012022-01-28C16284748780-1d6a99b39-9575-a426-e053-dadaa90af4c280395-203
80395-203-022022-01-28C16284748780-1d6a99b39-9575-a426-e053-dadaa90af4c280395-203

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80395-20380395-203-01, 80395-203-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
e173e20e-ef17-5721-e053-2995a90a4894ae4a61d9-edd7-21d5-e053-2995a90a096b2022-06-14WarningsExact identifier
spl set id: ae4a61d9-edd7-21d5-e053-2995a90a096b

Reported adverse events (FAERS/openFDA)#

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