PLAGENTRA BABY

Manufacturer
C.A Pharm Co., Ltd.
Effective date
2014-12-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:41:01

Label at a glance#

ProductPLAGENTRA BABY
Active ingredientGlycerin
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Glycerin 20%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Hydrogenated Polydecene, Dipropylene Glycol, Macadamia Integrifolia Seed Oil, Butylene Glycol, Cyclohexasiloxane, Betaine, Limnanthes Alba (Meadowfoam) Seed Oil, Stearic Acid, Glyceryl Stearate SE, Cyclopentasiloxane, Dimethiconol, Aloe Barbadensis Leaf Extract, Althaea Rosea Flower Extract, Arctium Lappa Root Extract, Artemisia Capillaris Leaf Extract, Calendula Officinalis Flower Extract, Lavandula Angustifolia (Lavender) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Ocimum Basilicum (Basil) Leaf Extract, Oenothera Biennis (Evening Primrose) Seed Extract, Perilla Frutescens Leaf Extract, Prunus Mume Fruit Extract, Thymus Vulgaris (Thyme) Extract, 1,2-Hexanediol, Portulaca Oleracea Extract, Hydrolyzed Collagen, Beta-Glucan, Ceramide 3, Raffinose, Palmitoyl Pentapeptide-4, Glyceryl Stearate, Olivoyl Hydrolyzed Wheat Protein, Cetearyl Alcohol, Glyceryl Oleate, Caprylic/Capric Glycerides, Dimethicone, Citrus Paradisi (Grapefruit) Fruit Extract, Polyglutamic Acid, Leuconostoc/Radish Root Ferment Filtrate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tocopheryl Acetate, Fragrance, Potassium Hydroxide, Disodium EDTA, Xanthan Gum

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Portectant

WARNINGS

WARNINGS SECTION

Warnings:
1. Stop using the product and go to a doctor immediately if one of the following symptoms occurs. If immediate care is not sought, the symptoms may worsen :
1) Itching, redness, swelling, rash, etc. 2) If one of the symptoms above occurs due to direct sunlight.
2. Do not apply the product to wounds or skin with dermatitis such as eczema.
3. Storage and Handling, 1) Keep the lid closed after use. 2) Keep the product out of children's reach. 3) Keep away from direct sunlight, do not store at high or low temperature.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of babies and children.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indication and usage:
1) Tighten the lid after using it.
2) Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight.
3) Use it in the morning or evening after shower.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and administration:
Take appropriate amount to the entire face and body, gently massage and tapping until absorbed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1483143glycerin 20 % Topical LotionPSN2
1483143glycerin 200 MG/ML Topical LotionSCD2
1483143glycerin 20 % Topical LotionSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130889422000122GTIN-13: 0889422000122
EAN-13: 0889422000122
GTIN-12: 889422000122
UPC-A: 889422000122
GTIN storage (14 digits): 00889422000122
plagentra baby carton.jpg
QR code linkQR Codewww.capharm.co.kr/plagentra baby carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68988-070-012020-01-31C16284748780-19d75b9d0-0e95-f424-e053-dadaa90a57ce3cf718cb-535c-4f03-bd47-ea26160f2861

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68988-070-01PLAGENTRA BABY100 mL in 1 CARTONLOTION1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68988-070PLAGENTRA BABY (GLYCERIN) LOTION [C.A PHARM CO., LTD.]2Legacy NDC, 1 package rows20141208_3cf718cb-535c-4f03-bd47-ea26160f2861.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GlycerinACTIVE INGREDIENTPDC6A3C0OX2
GLYCERINACTIVE MOIETYPDC6A3C0OX2
Dipropylene GlycolINACTIVE INGREDIENTE107L85C402
WaterINACTIVE INGREDIENT059QF0KO0R2

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
68988-07068988-070-01

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
GlycerinPDC6A3C0OXACTIB
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
fb018c88-d502-4095-a538-f8084fd671233cf718cb-535c-4f03-bd47-ea26160f28612014-12-08WarningsExact identifier
spl id: fb018c88-d502-4095-a538-f8084fd67123
spl set id: 3cf718cb-535c-4f03-bd47-ea26160f2861

Reported adverse events (FAERS/openFDA)#

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