VITA10 Brightening CapsuleMask

Manufacturer
C&TECH CORPORATION
Effective date
2017-08-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:14:20

Label at a glance#

ProductVITA10 Brightening CapsuleMask
Active ingredientGLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Step1(Mask): Glycerin

Step2(Ampoule): Glycerin

INACTIVE INGREDIENT SECTION

Step1: Water, Allantoin, etc.

Step2: Water, Biotin, Allantoin, Glycerin, etc.

OTC - PURPOSE SECTION

Skin Protectant - Moisture

WARNINGS SECTION

1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
1) Occurrence of red spots, swelling, itchiness, and other skin irritation
2) If the symptoms above occur after the application area is exposed to direct sunlight

2. Do not use on open wounds, eczema, and other skin irritations

3. Precaution for Storage and Handling
1) Close the lid after use
2) Keep out of reach of infants and children
3) Do not to store in a place with high/low temperature and exposed to direct sunlight

4. Use as avoiding eye areas.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

  1. Cleanse and tone face.
  2. Separate F1 (MG:gel mask) and F2 (Capsule Ampoule) by tearing along the dotted vertical line in the right side of the pouch.
  3. Fold F2 from the bottom 4~5 times and press it with your thumb. Please make sure move F2 over to F1 at the left,
  4. Gently rub the pouch to ensure F2 is penetrated into F1 completely.
  5. Open the pouch and place the mask on the face with the gel side contacting the skin.
  6. Gently remove the release fabric by grabbing the wing on the top of the mask. Use gel side of the mask to the face and dispose the release fabric.
  7. Leave the mask to the face and dispose the release fabric.
  8. Leave the mask about 20 minutes then remove.
  9. Lightly massage the remaining essence into the skin.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71621-000871621-0008-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
adffd988-c703-71fb-e053-2a95a90a60b255c0409c-86f8-238d-e054-00144ff88e882020-08-29WarningsExact identifier
spl set id: 55c0409c-86f8-238d-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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