TONYMOLY PANDAS DREAM WHITE HAND

Manufacturer: TONYMOLY CO.,LTD
Effective date: 2016-01-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:44:40

Label at a glance#

ProductTONYMOLY PANDAS DREAM WHITE HAND

Active ingredientNiacinamide

Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Niacinamide 2.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Butyrospermum Parkii (Shea) Butter, Glycerin, Cetyl Ethylhexanoate, Cetearyl Alcohol, Butylene Glycol, Glyceryl Stearate, Polysorbate 60, PEG/PPG-17/6 Copolymer, Cyclopentasiloxane, Hydrogenated Polydecene, Beeswax, Cyclohexasiloxane, Palmitic Acid, Stearic Acid, Xanthan Gum, Dimethicone, PEG-100 Stearate, Fragrance, Phenoxyethan ol, Tocopheryl Acetate, Polyacrylate-13, Chlorphenesin, Polyisobutene, Ethylhexylglycerin, Sorbitan Stearate, Caprylyl Glycol, Honey Extract, Phyllostachis Bambusoides Juice, Sorbitan Isostearate, Polysorbate 20, Disodium EDTA, Alcohol, Polyglutamic Acid, Citric Acid

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 routined

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of package

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1093331	niacinamide 2 % Topical Cream	PSN	1
1093331	niacinamide 20 MG/ML Topical Cream	SCD	1
1093331	niacinamide 2 % Topical Cream	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59078-220-01	2020-01-31	C162847	48780-1	9d75b9d0-53bc-f424-e053-dadaa90a57ce	608946b6-1770-4964-8248-f1a7288ed194

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59078-220-01	TONYMOLY PANDAS DREAM WHITE HAND	30 g in 1 PACKAGE	CREAM	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59078-220	TONYMOLY PANDAS DREAM WHITE HAND (NIACINAMIDE) CREAM [TONYMOLY CO.,LTD]	1	Legacy NDC, 1 package rows	20160120_608946b6-1770-4964-8248-f1a7288ed194.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

TONYMOLY PANDAS DREAM WHITE HAND
Niacinamide
Water
SHEA BUTTER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59078-220	59078-220-01

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
Name	UNII	Kind
Niacinamide	25X51I8RD4	ACTIB
Water	059QF0KO0R	IACT
SHEA BUTTER	K49155WL9Y	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
cbfe007c-f84a-4e70-b422-28d82e90e075			608946b6-1770-4964-8248-f1a7288ed194	2016-01-20	Warnings	Exact identifier spl id: cbfe007c-f84a-4e70-b422-28d82e90e075 spl set id: 608946b6-1770-4964-8248-f1a7288ed194

Reported adverse events (FAERS/openFDA)#

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