FDA.reportPublic FDA data

Airface Nicotinamide Facial Correcting Serum

Manufacturer
GUANGZHOU SHANGPIN BIOTECHNOLOGY CO.,LTD
Effective date
2024-07-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:16:13

Label at a glance#

ProductAirface Nicotinamide Facial Correcting Serum
Active ingredientALPHA-ARBUTIN, NIACINAMIDE, TRANEXAMIC ACID
Label structure12 sections

Dosage and administration

Take appropriate amount of this product, evenly apply to the skin, gently pat until absorbed. Twice a day.

Storage and handling

Store at room temperature, please store in a dry and ventilated place, away from direct sunlight.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

NIACINAMIDE 5%

TRANEXAMIC ACID 2%

ALPHA-ARBUTIN 1%

Purpose

OTC - PURPOSE SECTION

①Whitening &Removing spots ②Skin whitening ③Removin. spots

Use

INDICATIONS & USAGE SECTION

Take appropriate amount of this product, evenly apply to the skin, gently pat until absorbed. Twice a day.

Warnings

WARNINGS SECTION

1.For external use only.
2.Cases of papules and mild pruritus have been reported in arbutin.For the first time, try it behind
the ear or on the inside of the arm. If there is no abnormal problem, apply it to the face.
3. Do not use for children under 3 years old.

Do not use

OTC - DO NOT USE SECTION

Donnotuse on da maged skin(cuts, abrasionseczema, sunburn)f you are allergic to any of the ingredients in this product.

OTC - WHEN USING SECTION

1.When using this product keep out of eyes and mouth.

2.In case of contact with eyes, rinse eyes thoroughly with water:

3.It is not advised to use on areas with wounds and/or skin problems.
4.Stop use and ask a doctor if iritation or rash occurs. These may be signs of a serious condition.

5. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

6.Because this product contains a high concentration of active ingredients, the color of the product may change
slightly over time, which does not affect the efficacy and normal use of the product.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Take appropriate amount of this product, evenly apply to the skin, gently pat until absorbed. Twice a day.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature, please store in a dry and ventilated place, away from direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA,GLYCERIN.BUTYLENE GLYCOL ,ALOE BARBADENSIS LEAF JUICE,HYDROXYETHYL
UREA,YEAST EXTRACT,3-0-ETHYL ASCORBIC ACID,GENTIANA SCABRA ROOT EXTRACT,
AVENA SATIVA (OAT) KERNEL EXTRACT, PAEONIA LACTIFLORA EXTRACT,COLLAGEN,
TILIA CORDATA FLOWER EXTRACT,ALTHAEA OFFICINALIS ROOT EXTRACT,OL IGOPEPTIDE-1.
ARNICA MONTANA FLOWER EXTRACTSODIUM HYALURONATE,MAGNOLIA SIEBOLDII EXTRACT,
OLIGOPEPTIDE- 6,CYANOCOBAL AMIN,CITRIC ACID,LEUCONOSTOCRADISH ROOT FERMENT
FILTRATE,HYALURONIC ACID,1,2-HEXANEDIOL, PHENOXYETHANOL,PROPYLENE GLYCOL,
AMMONIUM ACRYLOYLDIME THYLTAURATE/VP COPOLYMER,STEARETH-21,STEARETH-2, .
HYDROXYETHYLPIPERAZINE ETHANE SULFONIC ACID,XANTHAN GUM,PENTYLENE GLYCOL,
PEG-10 DIMETHICONEMINYL DIMETHICONE CROSSPOLYMER,DIMETHICONE , ACETYL
TRIETHYL CITRATE,ETHYLHEXYLGLYCERIN, C13-16 ISOPARAFFIN,CETEARYL METHICONE,
PEG-40 STEARATE ,GLYCERYL ACRYLATE/ ACRYLIC ACID COPOLYMER,CAPRYLYL GLYCOL,
PVM/MA COPOLYMER,FRAGRANCE

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
TRANEXAMIC ACID Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
8234c772-5c41-424c-a33e-e06e8c4de9c1Product name220250626
fbe2ea47-480e-f5f1-0d64-c87fd5ac923bProduct name420250224
b82b4008-22fd-05f5-6cc6-c0a6e81c65b8Product name220240805
510b43a3-8143-a25f-19c6-476c90dbb618Product name920171115
d206bb34-ea65-399d-70d9-834f22dc2c18Product name320170724

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84581-002-012025-07-29C16284748780-13b156c62-2724-fb37-e063-e6dba90a4e0784251-002

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84581-002-01Airface Nicotinamide Facial Correcting Serum30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84581-002AIRFACE NICOTINAMIDE FACIAL CORRECTING SERUM LIQUID [GUANGZHOU SHANGPIN BIOTECHNOLOGY CO.,LTD]11 package rows20240731_1e1ece74-09d2-e7e8-e063-6294a90a7823.zip

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
84581-00284581-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 42 matching rows.

Name, UNII, Kind table
NameUNIIKind
FRAGRANCE FRESH CITRUS FLORAL ORC1501495OU4GI2R2WBIACT
COLLAGEN ALPHA-1(I) CHAIN BOVINEFB3DQM32F2IACT
ALOE VERA LEAFZY81Z83H0XIACT
OATZ6J799EAJKIACT
ALPHA-ARBUTIN72VUP07IT5ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
HYDROXYETHYL UREAMBQ7DDQ7ARIACT
NIACINAMIDE25X51I8RD4ACTIB
TRANEXAMIC ACID6T84R30KC1ACTIB
DIMETHICONE92RU3N3Y1OIACT
PENTYLENE GLYCOL50C1307PZGIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
HYALURONATE SODIUMYSE9PPT4THIACT
STEARETH-2153J3F32P58IACT
HYALURONIC ACIDS270N0TRQYIACT
HYDROXYETHYLPIPERAZINE ETHANE SULFONIC ACIDRWW266YE9IIACT
C13-16 ISOPARAFFINLED42LZG6OIACT
GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER (300000 CP AT 2%)MEA9KH24QGIACT
STEARETH-2V56DFE46J5IACT
ALTHAEA OFFICINALIS ROOTTRW2FUF47HIACT
PHENOXYETHANOLHIE492ZZ3TIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ACETYLTRIETHYL CITRATE5WBR36T90EIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GENTIANA SCABRA ROOTGXZ33VNT92IACT
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATED2QHA03458IACT
CAPRYLYL GLYCOL00YIU5438UIACT
PONCEAU 4RZ525CBK9PGIACT
CYANOCOBALAMINP6YC3EG204IACT
TILIA CORDATA FLOWERCFN6G1F6YKIACT
METHYL VINYL ETHER AND MALEIC ANHYDRIDE COPOLYMER (1100000 WAMW)T0VRI38HB0IACT
CETEARYL METHICONE (15000 MW)VY9RTR7MSYIACT
OLIGOPEPTIDE-10Q46328TRNKIACT
YEAST3NY3SM6B8UIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PEG-40 MONOSTEARATEECU18C66Q7IACT
XANTHAN GUMTTV12P4NEEIACT

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
1e1ece74-09d3-e7e8-e063-6294a90a78231e1ece74-09d2-e7e8-e063-6294a90a78232024-07-25WarningsExact identifier
spl id: 1e1ece74-09d3-e7e8-e063-6294a90a7823
spl set id: 1e1ece74-09d2-e7e8-e063-6294a90a7823

Reported adverse events (FAERS/openFDA)#

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