Skin-ion

Manufacturer: WAKO Korea Corp
Effective date: 2009-11-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:23:09

Label at a glance#

ProductSkin-ion

Active ingredientARBUTIN, ADENOSINE, GLYCERIN

Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

INGREDIENTS:

WATER, ARBUTIN, GLYCERIN, VITAMIN C, ADENOSINE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BOX LABEL

OTC - WHEN USING SECTION

DIRECTION OF USE:

1. Open cap fill water (liquid)

2. After 30 minutes, spray it

3. After use all, refill water (liquid)

DESCRIPTION SECTION

DESCRIPTION:

1. Whenever you want to feel freshed:

The Skin-Ion delivers a fine mist of reduced water that refreshes and hydrates dry, thirsty skin. Use several times a day to give yourself a revitalizing lift. In winter, rescue skin from overhead, dry indoor air. Skin-Ion's gentle mist will freshen your look without disturbing your makeup. At the beach or during sports, wash away perspiration and pollutants and restore skin to a natural and healthy pH.

2. Take Skin-Ion when you fly to avoid dry, dehydrated skin. Skin-Ion is even gentle enough for expectant mothers and the delicate skin of young babies. Simply mist the skin of your face, neck, arms and body several fines a day.

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
ADENOSINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813
GLYCERIN Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d676a241-be05-4740-b3ee-1a5f2ed422d2	Product name	4	20180615
dd8bd48f-20d6-43c7-b471-3ae872868afa	Product name	3	20180125
d41954ff-bc63-4b2c-aba0-9146707659d7	Product name	2	20151117

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49742-1001-1	2019-10-21	C162847	48780-1	956f9ecf-dd85-621f-e053-dbdaa90a74ad	6fc39322-244c-4f35-a983-c994ac17632a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49742-1001-1	Skin-ion	40 mL in 1 CARTON	SPRAY	40		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49742-1001	SKIN-ION (ARBUTIN, ADENOSINE, GLYCERIN) SPRAY [WAKO KOREA CORP]	1	Legacy NDC, 1 package rows	20100101_6fc39322-244c-4f35-a983-c994ac17632a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ADENOSINE	ACTIVE INGREDIENT	K72T3FS567	1
ARBUTIN	ACTIVE INGREDIENT	C5INA23HXF	1
GLYCERIN	ACTIVE INGREDIENT	PDC6A3C0OX	1
ADENOSINE	ACTIVE MOIETY	K72T3FS567	1
ARBUTIN	ACTIVE MOIETY	C5INA23HXF	1
GLYCERIN	ACTIVE MOIETY	PDC6A3C0OX	1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Skin-ion
ARBUTIN, ADENOSINE, GLYCERIN
ARBUTIN
ADENOSINE
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49742-1001	49742-1001-1

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
Name	UNII	Kind
ARBUTIN	C5INA23HXF	ACTIB
ADENOSINE	K72T3FS567	ACTIB
GLYCERIN	PDC6A3C0OX	ACTIB

Source Document#

Source XML · Source PDF

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
8089b888-7b55-44ea-a12a-6ab827edf4e8			6fc39322-244c-4f35-a983-c994ac17632a	2009-11-24		Exact identifier spl id: 8089b888-7b55-44ea-a12a-6ab827edf4e8 spl set id: 6fc39322-244c-4f35-a983-c994ac17632a

Reported adverse events (FAERS/openFDA)#

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