Label: SONATURAL THE PURE PORE TENSING CARBONIC BUBBLE POP CLAY MASK- kaolin cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71322-150-01, 71322-150-02 - Packager: Sonatural Global Co.,Ltd
- 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.
Drug Label Information
Updated November 29, 2017
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water, Sorbitol, Ammonium Lauryl Sulfate, Caprylic/Capric Triglyceride, Methyl Perfluorobutyl Ether, Methyl Perfluoroisobutyl Ether, Bentonite, Decyl Glucoside, Glycerin, Acrylates/Vinyl Neodecanoate Crosspolymer, Polysorbate 60, Titanium Dioxide, Fragrance, Beeswax, Chromium Oxide Greens, Potassium Hydroxide, Carbonated Water, Aloe Barbadensis Leaf Juice, Punica Granatum Fruit Extract, Portulaca Oleracea Extract, Camellia Sinensis Leaf Extract, Caprylyl Glycol, 1,2-Hexanediol, Propanediol, Illicium Verum (Anise) Fruit Extract, Phenoxyethanol, Chlorphenesin, Pyrus Malus (Apple) Fruit Extract, Hamamelis Virginiana (Witch Hazel) Bark/Leaf/Twig Extract
- PURPOSE
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WARNINGS
Warnings: 1. If the following symptoms occur, discontinue use and consult a dermatologist: 1) Red spots, swelling, itchiness, or irritation upon use 2) If above symptoms occur when skin is in direct sunlight 2. Do not use on open wounds and on skin with eczema or dermatitis 3. Storage instructions: 1) Keep out of reach of children 2) Store at room temperature away from direct sunlight 4. Avoid contact with eyes 5.Rinse with water immediately if the grain contact with eyes and stop use and ask a doctor if any symptoms occur 6. Use this product with dry hands
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SONATURAL THE PURE PORE TENSING CARBONIC BUBBLE POP CLAY MASK
kaolin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71322-150 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Kaolin (UNII: 24H4NWX5CO) (KAOLIN - UNII:24H4NWX5CO) Kaolin 45.5 g in 130 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Sorbitol (UNII: 506T60A25R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71322-150-02 1 in 1 CARTON 10/01/2017 1 NDC:71322-150-01 130 g in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2017 Labeler - Sonatural Global Co.,Ltd (694818511) Registrant - Sonatural Global Co.,Ltd (694818511) Establishment Name Address ID/FEI Business Operations ANCORS CO., LTD. 688494804 manufacture(71322-150)