PEPPLUS WRINKLE

Manufacturer
Picobio Co., Ltd
Effective date
2019-12-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:55:21

Label at a glance#

ProductPEPPLUS WRINKLE
Active ingredientDIMETHICONE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Dimethicone 3.35%

OTC - PURPOSE SECTION

Skin Protectant

INDICATIONS & USAGE SECTION

Prevent loss of skin elasticity and makes it healthy and lively

DOSAGE & ADMINISTRATION SECTION

 Take appropriate amount, apply gently to face and neck and tap it to absorb into the skin.

WARNINGS SECTION

For external use only.
Do not use on damaged or broken skin.
When using this product, keep out of eyes. Rinse with water to remove.
Stop using and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

INACTIVE INGREDIENT SECTION

Water, Dipropylene Glycol, Cetyl Ethylhexanoate, Squalane, Glyceryl Stearate,, Cetearyl Alcohol, Limnanthes Alba (Meadowfoam) Seed Oil, Polyacrylate-13, Polysorbate 60, Ethoxydiglycol, Sodium Hyaluronate, Trimethylpentanediol/Adipic Acid Copolymer, Sodium Stearoyl Glutamate, Hydrogenated Lecithin, Perilla Frutescens Leaf Extract, Nelumbo Nucifera Flower Extract, Chrysanthellum Indicum Extract, Chamomilla Recutita (Matricaris) Flower Extract, Hovenia Dulcis Fruit Extract, Solanum Lycopersicum (Tomato) Fruit/Leaf/Stem Extract, Lactobacillus ferment lysate, Mesembryanthemum Crystallinum Extract, Lactobacillus/Collagen Ferment Filtrate, 1,2-Hexanediol, Phenoxyethanol, PEG-10 Dimethicone/Vinyl Dimethicone Crosspolymer, Polyisobutene, Polysorbate 20, Carbomer, Triethanolamine, Adenosine, Tetrasodium EDTA, Tocopheryl Acetate, Dipotassium Glycyrrhizate, Copper Tripeptide-1, Acetyl Hexapeptide-8, Palmitoyl Pentapeptide-4, Tripeptide-1, Tripeptide-29, Hexapeptide-9, Hexapeptide-67 Palmitate, rh-Oligopeptide-1, Perfume

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72211-003-022021-11-02C16284748780-1ba0f9c33-5caf-a910-e053-dadaa90a0b8572211-003
72211-003-022021-01-29C16284748780-1ba0f9c33-5caf-a910-e053-dadaa90a0b8572211-003

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72211-00372211-003-01, 72211-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
cfd2b60f-025e-5d6e-e053-2995a90a503347029afb-613d-4411-8bad-f8c85c46318d2021-11-02WarningsExact identifier
spl set id: 47029afb-613d-4411-8bad-f8c85c46318d

Reported adverse events (FAERS/openFDA)#

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