TONYMOLY NATURALTH GOAT MILK WHITENING ESSENCE

Manufacturer
TONYMOLY CO.,LTD
Effective date
2016-01-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:44:41

Label at a glance#

ProductTONYMOLY NATURALTH GOAT MILK WHITENING ESSENCE
Active ingredientNiacinamide
Label structure8 sections

Dosage and administration

Directions: - clean the skin thoroughly before using - apply in daily skin care routine

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Niacinamide 2.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: goat milk extract, water, propanediol, dipropylene glycol, methylpropanediol, glycerin, piper methysticum leaf/root/stem extract, diphenyl dimethicone, triethylhexanoin, 1,2-hexanediol, arctium lappa root extract, centella asiatica extract, phellinus linteus extract, chamomilla recutita (matricaria) flower extract, rosmarinus officinalis (rosemary) leaf extract, hydrogenated lecithin, portulaca oleracea extract, phenoxyethanol, tromethamine, ethylhexylglycerin, sodium hyaluronate, xanthan gum, disodium edta, fragrance, polyglyceryl-10 myristate, carbomer, peg-40 hydrogenated castor oil, butylene glycol, calcium pantothenate, amylodextrin, folic acid, maltodextrin, hydrolyzed hyaluronic acid, ceramide 3, cholesterol, raffinose, sodium ascorbyl phosphate, pyridoxine hcl, silica, panthenol, palmitoyl pentapeptide-4, tocopheryl acetate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: For external use only

When using this product do not get into eyes

Stop use and ask a doctor if rash occurs

Do not use on - deep puncture wounds - animal bites - serious burns

Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Use

INDICATIONS & USAGE SECTION

Use: helps prevent and relieve chapped or cracked skin

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: - clean the skin thoroughly before using - apply in daily skin care routine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59078-260-012020-01-31C16284748780-19d75b9d0-d7e3-f424-e053-dadaa90a57ce3a567ae2-37eb-405d-af36-65cc16d5d9e9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59078-260-01TONYMOLY NATURALTH GOAT MILK WHITENING ESSENCE50 mL in 1 CARTONCREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59078-260TONYMOLY NATURALTH GOAT MILK WHITENING ESSENCE (NIACINAMIDE) CREAM [TONYMOLY CO.,LTD]2Legacy NDC, 1 package rows20160122_3a567ae2-37eb-405d-af36-65cc16d5d9e9.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
59078-26059078-260-01

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
Niacinamide25X51I8RD4ACTIB
goat milkXE5K5I4RP7IACT
water059QF0KO0RIACT

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
dcd3daaf-b761-41d9-85bb-c1c373e4e3493a567ae2-37eb-405d-af36-65cc16d5d9e92016-01-22WarningsExact identifier
spl id: dcd3daaf-b761-41d9-85bb-c1c373e4e349
spl set id: 3a567ae2-37eb-405d-af36-65cc16d5d9e9

Reported adverse events (FAERS/openFDA)#

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