AN ADC SP INTENSIVE MOISTURE ESSENCE

Manufacturer
AN Co Ltd.
Effective date
2016-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:22

Label at a glance#

ProductAN ADC SP INTENSIVE MOISTURE ESSENCE
Active ingredientNiacinamide
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Niacinamide 2.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Dipropylene Glycol, Phytosqualane, Glycerin, Phenyl Trimethicone, Panthenol, Cyclopentasiloxane/PEG-10 Dimethicone/Vinyl Dimechicone Cross Polymer, Cyclopentasiloxane, Hydrogenated Lecithin, 1,2-Hexanediol, Polyglyceryl-3 Methylglucose Distearate, Polyacrylamide/C13-14 Isoparaffin/ Laureth-7, CeramideNP/Hydrogenated Polydecene/Stearic Acid/ButyrospermumParkii(Shea) Butter/Ceteareth-20//Glyceryl Citrate/Lactate/Linoleate/Oleate Butylene glycol, Ethoxydiglycol, Trimethylpentanediol/Adipic Acid Copolymer, Sodium Polyacrylate, Phenoxyethanol, Beta-Glucan, Tocopheryl Acetate, Carbomer, Triethanolamine, Fragrance, Sodium Hyaluronate, Sodium Stearoyl Glutamate, Xanthan Gum, Disodium EDTA, Copper Tripeptide-1, Acetyl Hexapeptide-8, Palmitoyl Pentapeptide-4

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Precautions on use: 1. Stop using the product if there are any of the following abnormal symptoms appearing after use and consult with your dermatologist as continued use can worsen the symptoms. A) If there are red spots, swelling, itchiness, or irritation B) If the above symptoms appear around the skin to which the product has been applied after being exposed to direct sunlight. 2. Precautions on storage and handling A) Make sure to close the cap after use. B) Keep out of the reach of children. C) Do not keep the product in a hot or cold place or a place getting direct sunlight. 3. Do not apply the product to any parts of the skin with wound, eczema, or dermatitis.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Suggested use

INDICATIONS & USAGE SECTION

Suggested use: Nourish the skin with anti-wrinkle eye cream and apply an appropriate amount of the essence to the whole face and neck gently and evenly.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & administration: Apply 3~4g of essence to face evenly.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1093331niacinamide 2 % Topical CreamPSN1
1093331niacinamide 20 MG/ML Topical CreamSCD1
1093331niacinamide 2 % Topical CreamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69153-080-022023-01-30C16284748780-1f386c649-bed8-0266-e053-dadaa90a7c1a80861d31-100a-4c97-b9c7-afc3d8b3371a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69153-080-01AN ADC SP INTENSIVE MOISTURE ESSENCE55 g in 1 BOTTLE, PUMPCREAM551
69153-080-02AN ADC SP INTENSIVE MOISTURE ESSENCE1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69153-080AN ADC SP INTENSIVE MOISTURE ESSENCE (NIACINAMIDE) CREAM [AN CO LTD.]1Legacy NDC, 2 package rows20160624_80861d31-100a-4c97-b9c7-afc3d8b3371a.zip

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
69153-08069153-080-01, 69153-080-02

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
Niacinamide25X51I8RD4ACTIB
Water059QF0KO0RIACT
Dipropylene GlycolE107L85C40IACT

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
9a5141e2-b665-429e-b13d-82a7e84779b480861d31-100a-4c97-b9c7-afc3d8b3371a2016-06-24WarningsExact identifier
spl id: 9a5141e2-b665-429e-b13d-82a7e84779b4
spl set id: 80861d31-100a-4c97-b9c7-afc3d8b3371a

Reported adverse events (FAERS/openFDA)#

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