FDA.reportPublic FDA data

Miracle Aqua Peeling

Manufacturer
TOAS Co., Ltd.
Effective date
2018-09-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:56:50

Label at a glance#

ProductMiracle Aqua Peeling
Active ingredientHYALURONATE SODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium Hyaluronate 0.005%

OTC - PURPOSE SECTION

Moisturizing

INDICATIONS & USAGE SECTION

Helps to keep skin moistness

DOSAGE & ADMINISTRATION SECTION

Apply a generous amount on face and gently massage.
Rinse thoroughly.

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, 1,2-Hexanediol, Alcohol, Arginine, Butylene Glycol, Camellia Sinensis Leaf Extract, Canavalia Gladiata Seed Extract, Carbomer, Caviar Extract, Cellulose, Centella Asiatica Extract, Chamomilla Recutita (Matricaria) Flower Extract, Ethylhexylglycerin, Fragrance, Glycyrrhiza Glabra (Licorice) Root Extract, Nasturtium Offcinale Extract, PEG-400, PEG-60 Hydrogenated Castor Oil , Polygonum Cuspidatum Root Extract, Rosmarinus Officinalis (Rosemary) Leaf Exreact, Scutellaria Baicalensis Root Extract, Tocopheryl Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72557-001-012020-01-31C16284748780-19d75b9d0-642d-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72557-001-01Miracle Aqua Peeling100 g in 1 CONTAINERGEL1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72557-001MIRACLE AQUA PEELING (HYALURONATE SODIUM) GEL [TOAS CO., LTD.]2Legacy NDC, 1 package rows20180922_26bc7bd5-8a93-4891-8c8c-4ad6add9ded7.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72557-00172557-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ALCOHOL3K9958V90MIACT
ARGININE94ZLA3W45FIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
CAVIAR, UNSPECIFIED020K6HLU0OIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
HYALURONATE SODIUMYSE9PPT4THACTIB

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
7655e699-c7df-607e-e053-2991aa0aaf2426bc7bd5-8a93-4891-8c8c-4ad6add9ded72018-09-20WarningsExact identifier
spl id: 7655e699-c7df-607e-e053-2991aa0aaf24
spl set id: 26bc7bd5-8a93-4891-8c8c-4ad6add9ded7

Reported adverse events (FAERS/openFDA)#

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