AMULDY S

Manufacturer
Aloe Vera Korea Co.,Ltd.
Effective date
2021-07-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:46

Label at a glance#

ProductAMULDY S
Active ingredientGLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

glycerin

INACTIVE INGREDIENT SECTION

WATER, ALCOHOL, BUTYLENE GLYCOL, ETC

OTC - PURPOSE SECTION

for skin protectant

relieve itchiness by providing moisture and nutrients to the dry skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

shake the container for 2 to 3 times before use, apply it evenly

WARNINGS SECTION

■ if following abnormal symptoms occurs after use , stop use and consult with a skin specialist

red specks, swelling, itching

■ don’t use on the part where there is injury, eczema, or dermatitis

Keep out of reach of children

■ if swallowed, get medical help or contact a person control center immediately

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
82145-0001-12025-01-30C16284748780-12cef2736-9df1-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82145-0001-1AMULDY S50 mL in 1 BOTTLELIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82145-0001AMULDY S (GLYCERIN) LIQUID [ALOE VERA KOREA CO.,LTD.]1Legacy NDC, 1 package rows20210804_c8b14b2a-5ce0-3a33-e053-2a95a90a679f.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
82145-000182145-0001-1

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
WATER059QF0KO0RIACT
ALLANTOIN344S277G0ZIACT
GLYCERINPDC6A3C0OXACTIB

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
c8b14b2a-5ce1-3a33-e053-2a95a90a679fc8b14b2a-5ce0-3a33-e053-2a95a90a679f2021-07-29WarningsExact identifier
spl id: c8b14b2a-5ce1-3a33-e053-2a95a90a679f
spl set id: c8b14b2a-5ce0-3a33-e053-2a95a90a679f

Reported adverse events (FAERS/openFDA)#

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