K OXIDERM OP POST PROCEDURE SKIN CARE BRUISE- magnesium ascorbyl phosphate cream

K Oxiderm OP Post Procedure skin care bruise by

Drug Labeling and Warnings

K Oxiderm OP Post Procedure skin care bruise by is a Otc medication manufactured, distributed, or labeled by EZEKIELCOSMETIC CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Magnesium Ascorbyl Phosphate

INACTIVE INGREDIENT

water, propylene glycol, alcohol etc

PURPOSE

Reduces Discoloration on skin

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

for 4~5 days before cosmetic application, apply thinly twice a day, morning and night, after cleansing the skin

apply K oxiderm OP cream right after cosmetic application

K oxiderm OP cream is recommended for 10 to 15 days as preparatory skin care before and after surgical and medical cosmetic procedure

WARNINGS

1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
1) Occurrence of red spots, swelling, itchiness, and other skin irritation
2) If the symptoms above occur after the application area is exposed to direct sunlight
2. Do not use on open wounds, eczema, and other skin irritations
3. Precaution for Storage and Handling
1) Close the lid after use
2) Keep out of reach of infants and children
3) Do not to store in a place with high/low temperature and exposed to direct sunlight

4. Use as avoiding eye areas.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

K OXIDERM OP POST PROCEDURE SKIN CARE BRUISE 
magnesium ascorbyl phosphate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71588-0011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	MAGNESIUM ASCORBYL PHOSPHATE	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
MAGNESIUM PHOSPHIDE (UNII: Q846538H9E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71588-0011-1	30 mL in 1 TUBE; Type 0: Not a Combination Product	08/17/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/17/2017

Labeler - EZEKIELCOSMETIC CO., LTD (689851966)

Registrant - EZEKIELCOSMETIC CO., LTD (689851966)

Establishment
Name	Address	ID/FEI	Business Operations
EZEKIELCOSMETIC CO., LTD		689851966	label(71588-0011) , manufacture(71588-0011) , pack(71588-0011)