FDA.reportPublic FDA data

STEM CELL HMSC CELL REJUVENATION-AMPOULE

Manufacturer
BBHC CO., LTD | STC Nara Co., Ltd
Effective date
2022-01-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:16:19

Label at a glance#

ProductSTEM CELL HMSC CELL REJUVENATION-AMPOULE
Active ingredientNIACINAMIDE, ADENOSINE
Label structure11 sections

Indications and uses

Helps improve skin brightness and wrinkle care. Helps improve skin elasticity.

Dosage and administration

1) Wash your face thoroughly. Remove all makeups. 2) Directly apply the ampoule on your towel-dried face. 3) Remove the protection film from the bottle and screw open the lid. 4) Remove the innerprotection film in the container/bottle, insert the easy squirt, and remove the top silver lid and apply the ampoule on any intended area. 5) Allow enough amount of ampoule to get absorbed completely.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Niacinamide (2.00%)

Adenosine (0.04%)

Purpose

OTC - PURPOSE SECTION

Skin Brightening

Anti wrinkle

Uses

DOSAGE & ADMINISTRATION SECTION

  • Helps improve skin brightness and wrinkle care.
  • Helps improve skin elasticity.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INDICATIONS & USAGE SECTION

1) Wash your face thoroughly. Remove all makeups.

2) Directly apply the ampoule on your towel-dried face.

3) Remove the protection film from the bottle and screw open the lid.

4) Remove the innerprotection film in the container/bottle, insert the easy squirt, and remove the top silver lid and apply the ampoule on any intended area.

5) Allow enough amount of ampoule to get absorbed completely.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Human Umbilical Mesenchymal Stem Cell Conditioned Media, Glycerin, 1,2-Hexanediol, Caprylic/Capric Triglyceride, Cetyl Ethylhexanoate, Water, Glyceryl Acrylate/Acrylic Acid Copolymer, Propylene Glycol, Hydrogenated Lecithin, Polyglyceryl-10 Oleate, Sucrose Distearate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Propanediol, Caprylhydroxamic Acid, Sodium Hyaluronate, DNA, Carbomer, Sodium Chloride, Magnesium Aspartate, Zinc Gluconate, Copper Gluconate, Glucose, Cananga Odorata Flower Oil

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70ml NDC: 76731-208-01 Label70ml NDC: 76731-208-01 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76731-208-012022-12-30C16284748780-1e4f33bdf-a0b3-d8a0-e053-dadaa90a6e4e76731-208
76731-208-012022-07-29C16284748780-1e4f33bdf-a0b3-d8a0-e053-dadaa90a6e4e76731-208

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76731-20876731-208-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
GLYCERINPDC6A3C0OXIACT
CANANGA OIL8YOY78GNNXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
NIACINAMIDE25X51I8RD4ACTIB
MAGNESIUM ASPARTATER17X820ROLIACT
CETYL ETHYLHEXANOATE134647WMX4IACT
WATER059QF0KO0RIACT
POLYGLYCERYL-10 OLEATE55C81W76DHIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
PROPANEDIOL5965N8W85TIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
ADENOSINEK72T3FS567ACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
HYDROGENATED SOYBEAN LECITHINH1109Z9J4NIACT
SUCROSE DISTEARATE33X4X4B90SIACT
HYALURONATE SODIUMYSE9PPT4THIACT
SODIUM CHLORIDE451W47IQ8XIACT
ZINC GLUCONATEU6WSN5SQ1ZIACT
COPPER GLUCONATERV823G6G67IACT
ANHYDROUS DEXTROSE5SL0G7R0OKIACT

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
fbb624ce-4c3a-d321-e053-6394a90a73f8b2f390ce-07a1-3338-e053-2a95a90ab4ee2023-05-15WarningsExact identifier
spl set id: b2f390ce-07a1-3338-e053-2a95a90ab4ee

Reported adverse events (FAERS/openFDA)#

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