SEAWEED CLEANSING- mineral oil liquid

Seaweed Cleansing by

Drug Labeling and Warnings

Seaweed Cleansing by is a Otc medication manufactured, distributed, or labeled by AMAROS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Mineral Oil 50%

INACTIVE INGREDIENT

Inactive Ingredients: Water, Butylene Glycol, Polysorbate60, Cetyl Alcohol, Glycerin, Glyceryl Stearate SE, Sorbitan Sesquioleate, Dimethicone, Caprylyl Glycol / Caprylhydroxamic Acid, Carbomer, Triethanolamine, Allantoin, Xanthan Gum, Simmondsia Chinensis(Jojoba) Seed Oil, Sesamum Indicum (Sesame) Seed Oil, Triticum Vulgare (Wheat) Germ Oil, Algae Extract, Carica Papaya (Papaya) Leaf Extract, Ascorbic acid, Fragrance, CI 42053.

PURPOSE

Purpose: Skin protectant

WARNINGS

Warnings: 1. In case of having following symptoms after using this product, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist . 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children: Keep out of reach of babies and children.

INDICATIONS AND USAGE

Indication and Usage: 1. Tighten the lid after using it. 2. Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight.3. Use it in the morning or evening.

DOSAGE AND ADMINISTRATION

Dosage and Administration: Apply an appropriate amount on face and rub it into skin by massage method. Wipe up face with warm water. Cleansing cream gently removes tough waterproof make up.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SEAWEED CLEANSING 
mineral oil liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60899-050
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Mineral Oil (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP)	Mineral Oil	75 mg  in 150 mL

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: 60899-050-01	150 mL in 1 CARTON; Type 0: Not a Combination Product	09/01/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	09/01/2013

Labeler - AMAROS CO., LTD. (690338801)

Registrant - AMAROS CO., LTD. (690338801)

Establishment
Name	Address	ID/FEI	Business Operations
AMAROS CO., LTD.		690338801	manufacture(60899-050)