AN ADC SP INTENSIVE WRINKLE

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 WRINKLE
Active ingredientDimethicone
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Dimethicone 1.3%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Butylene Glycol, Cyclopentasiloxane/PEG-10 Dimethicone/Vinyl Dimechicone Cross Polymer, Dipropylene Glycol, Olive Oil Glycereth-8 Esters, Panthenol, Cetyl Ethylhexanoate, Phytosqualane, 1,2-Hexanediol, Cetyl Alcohol, Glyceryl Stearate, Limnanthes Alba (Meadowfoam) Seed Oil, Polyacrylamide/C13-14 Isoparaffin/ Laureth-7, Polysorbate 60, Ethoxydiglycol, Trimethylpentanediol/Adipic Acid Copolymer, CeramideNP/Hydrogenated Polydecene/Stearic Acid/ButyrospermumParkii(Shea) Butter/Ceteareth-20/Glyceryl Citrate/Lactate/Linoleate/Oleate Butylene glycol, Phenoxyethanol, Beta-Glucan, Dipotassium Glycyrrhizate, Fragrance, Sodium Stearoyl Glutamate, Hydrogenated Lecithin, Carbomer, Triethanolamine, Sodium Polyacrylate, Tocopheryl Acetate, Xanthan Gum, Adenosine, Disodium EDTA, Sodium Hyaluronate, Copper Tripeptide-1, Palmitoyl Pentapeptide-4, Acetyl Hexapeptide-8

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: At the final stage of basic makeup, apply an appropriate amount of the cream to the whole face and gently massage the face upwards to help the skin absorb the nutrients.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & administration: Apply 3~4g of cream to the whole face evenly.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
309916dimethicone 1.3 % Topical CreamPSN1
309916dimethicone 13 MG/ML Topical CreamSCD1
309916dimethicone 0.65 GM per 50 ML Topical CreamSY1
309916dimethicone 1.3 % Topical CreamSY1
309916dimethicone 1.95 GM per 150 ML Topical CreamSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIMETHICONE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69153-100-022023-01-30C16284748780-1f386c64a-3242-0266-e053-dadaa90a7c1a43d013b4-edc5-44be-a35a-c5d0d82e70b9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69153-100-01AN ADC SP INTENSIVE WRINKLE50 g in 1 BOTTLE, GLASSCREAM501
69153-100-02AN ADC SP INTENSIVE WRINKLE1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69153-100AN ADC SP INTENSIVE WRINKLE (DIMETHICONE) CREAM [AN CO LTD.]1Legacy NDC, 2 package rows20160624_43d013b4-edc5-44be-a35a-c5d0d82e70b9.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
69153-10069153-100-01, 69153-100-02

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
Dimethicone92RU3N3Y1OACTIB
Water059QF0KO0RIACT
Butylene Glycol3XUS85K0RAIACT

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
608b9fe3-2c34-4da4-868b-00badce3656c43d013b4-edc5-44be-a35a-c5d0d82e70b92016-06-24WarningsExact identifier
spl id: 608b9fe3-2c34-4da4-868b-00badce3656c
spl set id: 43d013b4-edc5-44be-a35a-c5d0d82e70b9

Reported adverse events (FAERS/openFDA)#

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