FDA.reportPublic FDA data

Obeo 7way Moisture

Manufacturer
CPbio Co., Ltd
Effective date
2016-01-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:43

Label at a glance#

ProductObeo 7way Moisture
Active ingredientGLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Glyerin 8.00%

OTC - PURPOSE SECTION

Skin Protectant

INDICATIONS & USAGE SECTION

Helps to prevent dehydration of skin

DOSAGE & ADMINISTRATION SECTION

Apply liberally as needed onto skin

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

Stop using and ask a doctor if rash occurs

When using this product, keep out of eyes. Rinse with water to remove

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Water, Xanthan Gum, Disodium EDTA, Butylene Glycol, Triethanolamine, Hydrogenated C6-14 Olefin Polymers, Caprylic/Capric Triglyceride, Polysorbate 60, Butyrospermum Parkii (Shea) Butter, Hydrogenated Lecithin, Stearic acid, Sorbitan Stearate, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Carbomer, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 80, Caprylhydroxamic Acid, 1,2-Hexanediol, Caprylyl Glycol, Boswellia Serrata Resin Extract, Fragrance, Mineral Water, Sodium Hyaluronate, Propandiol, Saccharomyces/Viscum Album (Mistletoe) Ferment Extract, Saccharomyces/Imperata Cylindrica Root Ferment Extract, Lactobacillus/Soybean Ferment Extract, Human Oligopeptide-1, Caprylyl Glycol, Oryza Sativa (Rice) Callus Culture Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69871-003-022020-01-31C16284748780-19d75b9d0-5422-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69871-003-01Obeo 7way Moisture200 mL in 1 CONTAINERLOTION2001
69871-003-02Obeo 7way Moisture1 in 1 CARTONLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69871-003OBEO 7WAY MOISTURE (GLYCERIN) LOTION [CPBIO CO., LTD]1Legacy NDC, 2 package rows20160125_74782c1c-e3d9-4083-b2fb-3bb7cff375ef.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69871-00369871-003-01, 69871-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXACTIB
WATER059QF0KO0RIACT
XANTHAN GUMTTV12P4NEEIACT
EDETATE DISODIUM7FLD91C86KIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
TROLAMINE9O3K93S3TKIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
POLYSORBATE 60CAL22UVI4MIACT
SHEA BUTTERK49155WL9YIACT
HYDROGENATED SOYBEAN LECITHINH1109Z9J4NIACT
STEARIC ACID4ELV7Z65APIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)1DXE3F3OZXIACT
ISOHEXADECANE918X1OUF1EIACT
POLYSORBATE 806OZP39ZG8HIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
CAPRYLYL GLYCOL00YIU5438UIACT
INDIAN FRANKINCENSE4PW41QCO2MIACT
HYALURONATE SODIUMYSE9PPT4THIACT
PROPANEDIOL5965N8W85TIACT
VISCUM ALBUM FRUITING TOPBK9092J5MPIACT
IMPERATA CYLINDRICA ROOTVYT2JA85NHIACT

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
69200821-247e-49a9-b071-45da086721ed74782c1c-e3d9-4083-b2fb-3bb7cff375ef2016-01-25WarningsExact identifier
spl id: 69200821-247e-49a9-b071-45da086721ed
spl set id: 74782c1c-e3d9-4083-b2fb-3bb7cff375ef

Reported adverse events (FAERS/openFDA)#

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