LIMULUS BIO CELLULOSE MASK- glycerin, niacinamide, adenosine kit

Limulus Bio Cellulose Mask by

Drug Labeling and Warnings

Limulus Bio Cellulose Mask by is a Otc medication manufactured, distributed, or labeled by Skin R&D, SLC CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Glycerin, Niacinamide, Adenosine

INACTIVE INGREDIENT

Water, Butylene Glycol, etc

PURPOSE

Wrinkle Care, Whitening, AC Care

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of the children

INDICATIONS & USAGE

1. Open the package and unfold the cellulose mask pack. Then, remove the white film.
2. Attach the product tightly on your face using the side where the white film was removed. Then, remove the fabric on the other side.
3. Carefully adjust the position of the mask on your face. Try not to damage the soft cellulose mask pack.
4. After taking 20-30 minutes of rest, remove the mask. Let your skin absorb the remaining essence with gently dabbing motion.

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIMULUS BIO CELLULOSE MASK 
glycerin, niacinamide, adenosine kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71464-0004

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71464-0004-1	1 in 1 PACKAGE; Type 0: Not a Combination Product	06/28/2017

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 POUCH	28 g
Part 2	1 POUCH	28 g
Part 3	1 POUCH	28 g

Part 1 of 3

LIMULUS BIO CELLULOSE MASK WRINKLE CARE 
adenosine liquid

Product Information
Item Code (Source)	NDC: 71464-0005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.04 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71464-0005-1	28 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/28/2017

Part 2 of 3

LIMULUS BIO CELLULOSE MASK WHITENING 
niacinamide liquid

Product Information
Item Code (Source)	NDC: 71464-0006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71464-0006-1	28 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/28/2017

Part 3 of 3

LIMULUS BIO CELLULOSE MASK AC CARE 
glycerin liquid

Product Information
Item Code (Source)	NDC: 71464-0007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	16 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71464-0007-1	28 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	06/28/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/28/2017

Labeler - Skin R&D (694792365)

Registrant - Skin R&D (694792365)

Establishment
Name	Address	ID/FEI	Business Operations
SLC CO.,LTD.		694477505	manufacture(71464-0005, 71464-0004, 71464-0006, 71464-0007)

Establishment
Name	Address	ID/FEI	Business Operations
Skin R&D		694792365	label(71464-0004, 71464-0005, 71464-0006, 71464-0007)