Bano Water Glow InjectionMask

Manufacturer
Banobagi Co., Ltd. | Cntec inc
Effective date
2018-01-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:05:10

Label at a glance#

ProductBano Water Glow InjectionMask
Active ingredientGLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Glycerin

INACTIVE INGREDIENT SECTION

Water, allantoin, etc

OTC - PURPOSE SECTION

Skin Protectant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

1. After cleansing your face, apply some skin toner

2. Take the product out of the pouch and adhere it evenly over your face avoiding the eye and mouth area.

3. Remove it after 10~20 minutes.

4. Using your fingers, gently pat any remaining product into the skin until thoroughly absorbed.

WARNINGS SECTION

1. Please stop using the product for the following symptoms and it is advised to consult a dermatologist when it gets worse.

a)Red dots, swelling, itching or irritation while using the product.

b)Above symptoms at direct sunlight.

2. Please do not apply on the wounded, eczema or inflammation area.

3. Storage & Handling

a)Please keep away from infants and little children,

b)Please do not keep at extremely high or low temperature or under direct sunlight.

4. Please avoid using around eye circles.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72001-0004-12022-01-11C16284748780-19d75b9d1-1e3c-f424-e053-dadaa90a57ceDrug Facts
72001-0004-12020-01-31C16284748780-19d75b9d1-1e3c-f424-e053-dadaa90a57ceDrug Facts

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72001-000472001-0004-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALLANTOIN344S277G0ZIACT
GLYCERINPDC6A3C0OXACTIB

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
d5477640-4af0-5ebe-e053-2995a90a6e7e6279eef3-7688-bedd-e053-2991aa0ad9b12022-01-10WarningsExact identifier
spl set id: 6279eef3-7688-bedd-e053-2991aa0ad9b1

Reported adverse events (FAERS/openFDA)#

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