FDA.reportPublic FDA data

SUPER AQUA MAX WHITE C WATERFUL TONER

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2012-09-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:45:44

Label at a glance#

ProductSUPER AQUA MAX WHITE C WATERFUL TONER
Active ingredientGlycerin
Label structure8 sections

Indications and uses

How to Use: After washing your face, dispense an appropriate amount onto a cotton pad or onto your hand and apply it to your entire face. Gently pat your face to enhance its absorption into your skin.

Dosage and administration

How to Use: After washing your face, dispense an appropriate amount onto a cotton pad or onto your hand and apply it to your entire face. Gently pat your face to enhance its absorption into your skin.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Glycerin 20%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Dipropylene Glycol, PEG-8, Niacinamide, Phenoxyethanol, Biosaccharide Gum-1, Myrciaria Dubia Fruit Extract, PEG-40 Hydrogenated Castor Oil, PPG-26-Buteth-26, Caprylyl Glycol, Citrus Aurantium Dulcis (Orange) Fruit Water, Fragrance(Parfum), Carbomer, Arginine, Sodium Hyaluronate, Disodium EDTA, Honey Extract, Butylene Glycol, Trichosanthes Kirilowii Root Extract, Oenothera Biennis (Evening Primrose) Flower Extract, Ipomoea Purpurea Extract, Mirabilis Jalapa Extract, Avena Sativa (Oat) Kernel Extract, Rubus Idaeus (Raspberry) Leaf Extract, Calendula Officinalis Flower Extract, Nepeta Cataria Extract, Stellaria Media (Chickweed) Extract, Baptisia Tinctoria Root Extract, Sodium Polyacrylate, Hedera Helix (Ivy) Leaf/Stem Extract, Phytic Acid, PPG-1-PEG-9 Lauryl Glycol Ether, Helianthus Annuus (Sunflower) Seed Extract, Ascorbyl Glucoside

PURPOSE

OTC - PURPOSE SECTION

Purpose: Highly moisturizing brigtening toner

WARNINGS

WARNINGS SECTION

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rash appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

How to Use:
After washing your face, dispense an appropriate amount onto a cotton pad or onto your hand and apply it to your entire face.
Gently pat your face to enhance its absorption into your skin.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use:
After washing your face, dispense an appropriate amount onto a cotton pad or onto your hand and apply it to your entire face.
Gently pat your face to enhance its absorption into your skin.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-127-012021-06-30C16284748780-19d75b9cf-d7f6-f424-e053-dadaa90a57cefa0faafa-b231-4447-b8d8-2501914e3915
51346-127-012020-01-31C16284748780-19d75b9cf-d7f6-f424-e053-dadaa90a57cefa0faafa-b231-4447-b8d8-2501914e3915

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GlycerinACTIVE INGREDIENTPDC6A3C0OX1
GlycerinACTIVE MOIETYPDC6A3C0OX1
Caprylyl GlycolINACTIVE INGREDIENT00YIU5438U1
Dipropylene GlycolINACTIVE INGREDIENTE107L85C401
NiacinamideINACTIVE INGREDIENT25X51I8RD41
PhenoxyethanolINACTIVE INGREDIENTHIE492ZZ3T1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-12751346-127-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
GlycerinPDC6A3C0OXACTIM
Water059QF0KO0RIACT
Dipropylene GlycolE107L85C40IACT
Niacinamide25X51I8RD4IACT
PhenoxyethanolHIE492ZZ3TIACT
Caprylyl Glycol00YIU5438UIACT

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 · 13 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL / TOPICAL1.05 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
NiacinamideNIACINAMIDE25X51I8RD4INJECTION / INTRAMUSCULAR2.5 %w/vExact identifier — unii candidate
4 equally ranked IID candidates
NiacinamideNIACINAMIDE25X51I8RD4CREAM / TOPICALNAExact identifier — unii candidate
4 equally ranked IID candidates
NiacinamideNIACINAMIDE25X51I8RD4GEL / TOPICAL25 mgExact identifier — unii candidate
4 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL, FOAM / TOPICAL72 mgExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM, AUGMENTED / TOPICAL10 mgExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM / TOPICAL57 mgExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
3 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
3 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TGEL / TOPICAL14 mgExact identifier — unii candidate
6 equally ranked IID candidates
NiacinamideNIACINAMIDE25X51I8RD4INJECTION / INTRAVENOUS2.5 %w/vExact identifier — unii candidate
4 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
b31c4749-f21c-4d3e-b8d5-5f6487086db8fa0faafa-b231-4447-b8d8-2501914e39152021-06-29WarningsExact identifier
spl set id: fa0faafa-b231-4447-b8d8-2501914e3915

Reported adverse events (FAERS/openFDA)#

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