OTC Medication Information: KAEWOON FOR MEN

KAEWOON FOR MEN- hyaluronic acid and allantoin gel
RNCARE

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.

HYALURONIC ACID 2%

Allantoin 0.2%

Skin Protectant

Body Cleansing

Take an appropriate amount and massage onto body for about 60 seconds and rinse with water

In case of eye contact, immediately rinse with water

Stop use if unusual redness, swelling, soreness or irritation occur

Keep out of reach of children

Water, Polyquaternium-10 , Hydroxyethylcellulose , Black Strap Powder , Oleic Acid , Menthol , Lauryl Glucoside , Polysorbate 85 , 1,2-Hexanediol , Caprylic/Capric Triglyceride , Oryza Sativa (Rice) Bran Extract , Curcuma Longa (Turmeric Root) Extract, Vigna Radiata Seed Extract , Artemisia Princeps Extract , Arctium Lappa Root Extract , Hippophae Rhamnoides Extract , Hawthorn Crataegus Cuneata Extract Rheum Palmatum Root Extract , Bambusa Vulgaris Extract, Hamamelis Virginiana (Witch Hazel) Extract , Chamomilla Recutita (Matricaria) Extract , Panax Ginseng Root Extract , Propolis Extract , Sapindus Mukurossi Fruit Extract , Disodium EDTA , Diglycerin , Hydrolyzed Collagen , Butylene Glycol , Lauramidopropyl Betaine , Shea Butteramidopropyl Betaine , Capryl/Capramidopropyl Betaine , Sodium Cocoamphoacetate , Fragrance

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KAEWOON FOR MEN
hyaluronic acid, allantoin gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71237-003
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYALURONIC ACID (HYALURONIC ACID) HYALURONIC ACID 20 mg in 1 mL
ALLANTOIN (ALLANTOIN) ALLANTOIN 2 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)
MENTHOL, UNSPECIFIED FORM
LAURYL GLUCOSIDE
POLYSORBATE 85
1,2-HEXANEDIOL
MEDIUM-CHAIN TRIGLYCERIDES
RICE BRAN
TURMERIC
MUNG BEAN
ARCTIUM LAPPA ROOT
HIPPOPHAE RHAMNOIDES SEED
RHEUM PALMATUM ROOT
BAMBUSA VULGARIS WHOLE
HAMAMELIS VIRGINIANA LEAF WATER
MATRICARIA CHAMOMILLA ROOT
SAPINDUS MUKOROSSI FRUIT
EDETATE DISODIUM ANHYDROUS
BUTYLENE GLYCOL
LAURAMIDOPROPYL BETAINE
SODIUM COCOAMPHOACETATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71237-003-02 1 BOTTLE in 1 CARTON contains a BOTTLE (71237-003-01)
1 NDC:71237-003-01 320 mL in 1 BOTTLE This package is contained within the CARTON (71237-003-02)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 11/21/2018
Labeler — RNCARE (694893883)
Registrant — RNCARE (694893883)
Establishment
Name Address ID/FEI Operations
RNCARE 694893883 manufacture (71237-003)

Revised: 12/2019 RNCARE

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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