OTC Medication Information: K Oxiderm OP Post Procedure Skin Care Bruise

K OXIDERM OP POST PROCEDURE SKIN CARE BRUISE- magnesium ascorbyl phosphate cream
EZEKIELCOSMETIC CO., LTD

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Magnesium Ascorbyl Phosphate

water, propylene glycol, alcohol etc

Reduces Discoloration on skin

keep out of reach of the children

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

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.

for external use only

label
(click image for full-size original)

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 DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MAGNESIUM ASCORBYL PHOSPHATE (ASCORBIC ACID) MAGNESIUM ASCORBYL PHOSPHATE 0.5 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
ALCOHOL
MAGNESIUM PHOSPHIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71588-0011-1 30 mL in 1 TUBE None
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 Operations
EZEKIELCOSMETIC CO., LTD 689851966 label (71588-0011), manufacture (71588-0011), pack (71588-0011)

Revised: 08/2017 EZEKIELCOSMETIC CO., LTD

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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