Label: DR PORE TIGHTENING PINK CLAY FACIAL MASK- kaolin cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69457-060-01, 69457-060-02 - Packager: LAB & Company Inc.
- 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 December 7, 2017
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water, Ethylhexyl Palmitate, Calamine, Butylene Glycol, Glycerin, Cetyl Alcohol, Beeswax, 1,2-Hexanediol, Polysorbate 60, Glyceryl Stearate, Sorbitan Stearate, Stearic Acid, PEG-100 Stearate, Stearyl Alcohol, Prunus Serrulata Flower Extract, Camellia Japonica Flower Extract, Nelumbo Nucifera Flower Extract, Ethylhexylglycerin, Aloe Barbadensis Leaf Extract, Bioflavonoids, Brassica Oleracea Italica (Broccoli) Extract, Propanediol, Butyrospermum Parkii (Shea) Butter, Simmondsia Chinensis (Jojoba) Seed Oil, Tocopheryl Acetate, Myristyl Alcohol, Glyceryl Caprylate, Allantoin, Lauryl Alcohol, Cetearyl Alcohol, Arginine, Xanthan Gum, Carbomer, Dimethicone, Illite, Disodium EDTA, Fragrance
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- QUESTIONS
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR PORE TIGHTENING PINK CLAY FACIAL MASK
kaolin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69457-060 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Kaolin (UNII: 24H4NWX5CO) (KAOLIN - UNII:24H4NWX5CO) Kaolin 4.0 g in 100 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69457-060-02 1 in 1 CARTON 11/01/2017 1 NDC:69457-060-01 100 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 OTC monograph final part347 11/01/2017 Labeler - LAB & Company Inc. (688284779) Registrant - LAB & Company Inc. (688284779) Establishment Name Address ID/FEI Business Operations Natuzen Co.,Ltd. 688201272 manufacture(69457-060)