SHIELDLIFE COLLAGEN ION MASK- adenosine patch

Shieldlife Collagen Ion Mask by

Drug Labeling and Warnings

Shieldlife Collagen Ion Mask by is a Otc medication manufactured, distributed, or labeled by Orion Electronics Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Adenosine

INACTIVE INGREDIENT

WATER, GLYCERIN, BUTYLENE GLYCOL, ETC.

PURPOSE

Skin protectant

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

1. Gently and thoroughly wash face.

2. Place mask on face using the eye openings to center the mask.

3. Remove mask after 15-20 minutes and gently pat in any remaining treatment into the skin.

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)

2.Side Effects

1)Due to the use of this product, if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your pharmacist 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

SHIELDLIFE COLLAGEN ION MASK 
adenosine patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71118-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	1 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: 71118-0001-1	25 g in 1 POUCH; Type 0: Not a Combination Product	10/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/13/2016

Labeler - Orion Electronics Inc. (033245247)

Registrant - Orion Electronics Inc. (033245247)

Establishment
Name	Address	ID/FEI	Business Operations
Orion Electronics Inc.		033245247	manufacture(71118-0001)