Label: BK CELL AQUA PERFECT SNAIL- dimethicone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69946-060-01 - Packager: BNK CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 15, 2015
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Snail Secretion Filtrate, Cetyl Ethylhexanoate, Butylene Glycol, Pentaerythrityl Tetraethylhexanoate, Glycerin, Squalane, Cyclopentasiloxane, Niacinamide, Hydrogenated Polydecene, Cetearyl Alcohol, Propanediol, Cetearyl Glucoside, Beta-Glucan, Sodium Hyaluronate, Trehalose, Betaine, Dimethiconol, Glyceryl Stearate, PEG-100 Stearate, Triethanolamine, Carbomer, Phenoxyethanol, Ethylhexylglycerin, Adenosine, Flavor, Disodium EDTA, Malus Domestica Fruit Cell Culture Extract, Morus Alba Leaf Extract, Camellia Sinensis Leaf Extract, Centella Asiatica Extract, Rosa Centifolia Flower Water, Portulaca Oleracea Extract
- PURPOSE
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WARNINGS
Warnings: 1. In case of having following symptoms after using this, 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
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BK CELL AQUA PERFECT SNAIL
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69946-060 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) Dimethicone 0.5 g in 50 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Cetyl Ethylhexanoate (UNII: 134647WMX4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69946-060-01 50 g in 1 CARTON; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 06/01/2015 Labeler - BNK CO., LTD. (689515209) Registrant - BNK CO., LTD. (689515209) Establishment Name Address ID/FEI Business Operations BNK CO., LTD. 689515209 manufacture(69946-060)
