Label: ALOE BHA SKIN TONER- glycerin liquid
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Updated August 16, 2016
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- ACTIVE INGREDIENT
Inactive Ingredients: Aloe Barbadensis Leaf Water, Sodium Hyaluronate, Snail Secretion Filtrate, Pentylene Glycol, Zanthoxylum Piperitum Fruit Extract, Pulsatilla Koreana Extract, Usnea Barbata (Lichen) Extract, Polysorbate 20, Salicylic Acid, Arginine, Althaea Rosea Flower Extract, Aloe Barbadensis Leaf Extract, Aloe Barbadensis Leaf Juice, Beta-Glucan, Polyglutamic Acid, Aspalathus Linearis Extract, Portulaca Oleracea Extract, Psidium Guajava Fruit Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum
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. 4. Do not use this for children under three because it contains salicylic acid and salts.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
ALOE BHA SKIN TONER
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69998-090 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin 5.2 g in 200 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) Pentylene Glycol (UNII: 50C1307PZG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69998-090-02 1 in 1 CARTON 07/01/2016 1 NDC:69998-090-01 200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2016 Labeler - BENTON KOREA (689514965) Registrant - BENTON KOREA (689514965) Establishment Name Address ID/FEI Business Operations BENTON KOREA 689514965 repack(69998-090) Establishment Name Address ID/FEI Business Operations Ezekiel Cosmetics Co. 689061889 manufacture(69998-090)