REVERDIR PTD Black Diamond Mask

Manufacturer
AD BIOTECH CO.,LTD
Effective date
2019-12-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:50:24

Label at a glance#

ProductREVERDIR PTD Black Diamond Mask
Active ingredientAllantoin
Label structure8 sections

Indications and uses

Indication and Usage: After washing face, at the first stage of skin care, wet cotton pad with product and lightly tap on face.

Dosage and administration

Dosage and Administration: Take an adequate amount of this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Allantoin 0.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Purified Water, Aloe Barbadensis Leaf Extract, Dipropylene Glycol, Citrus Unshiu Peel Extract(100ppm), Butylene Glycol, Niacinamide, Camellia Sinensis Leaf Extract, Charcoal Powder, Chondrus Crispus (Carrageenan), Ceratonia Siliqua Gum, Algae Extract, Cyamopsis Tetragonoloba (Guar) Gum, Glucose, Glycine Soja(Soybean) Phytoplacenta Extract, Diamond Powder(100ppm dilute solution), Potassium Chloride, Fragrance, Ethylhexylglycerin, Rose Extract, Ubiquinone, Pearl Powder, Collagen, Tocopheryl Acetate, Rosa Centifolia Flower Water, Punica Granatum Fruit Extract, Disodium EDTA, Glycine Soja (Soybean) Seed Extract, Rubus Fruticosus(Blackberry) Fruit Extract, Adenosine, Oligopeptide -91 rh-Oligopeptide-1 sodium Carbonate Trehalose, trehalose fh-polypeptide-11 dipeptide-19 oligopeptide-91 Hexapeptide-40, Snail Secretion Filtrate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warning: 1. In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of Children: Keep out of reach of babies and children

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Indication and Usage: After washing face, at the first stage of skin care, wet cotton pad with product and lightly tap on face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and Administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cello packImage of cello packImage of cello packImage of cello pack

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AllantoinACTIVE INGREDIENT344S277G0Z1
ALLANTOINACTIVE MOIETY344S277G0Z1
Dipropylene GlycolINACTIVE INGREDIENTE107L85C401
WaterINACTIVE INGREDIENT059QF0KO0R1

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
61098-01061098-010-01

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
Allantoin344S277G0ZACTIB
Water059QF0KO0RIACT
Dipropylene GlycolE107L85C40IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
3 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
3 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40SYSTEM / TRANSDERMAL6 mgExact identifier — unii candidate
3 equally ranked IID candidates

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
1bcec454-942e-448d-b6ae-c328f6f8d33a66e97256-1e8a-4bb1-a4c4-a32be7db3ebe2021-06-04WarningsExact identifier
spl set id: 66e97256-1e8a-4bb1-a4c4-a32be7db3ebe

Reported adverse events (FAERS/openFDA)#

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