Label: CLEMATIS MORNING DEW BB 21 LIGHT BEIGE- titanium dioxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71702-090-01, 71702-090-02 - Packager: Coshub Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 September 5, 2017
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water, Cyclopentasiloxane, Phenyl Trimethicone, Cyclohexasiloxane, Dimethicone, Butylene Glycol, Butylene Glycol Dicaprylate/Dicaprate, PEG-10 Dimethicone, Glycerin, Niacinamide, Dicaprylyl Carbonate, Methyl Methacrylate Crosspolymer, Sodium Chloride, Disteardimonium Hectorite, Ozokerite, Trimethylsiloxyphenyl Dimethicone, Hydrogenated Polydecene, Hydrogenated Polyisobutene, Iron Oxides(CI77492), Dimethicone/Vinyl Dimethicone Crosspolymer, Cetyl Peg/Ppg-10/1 Dimethicone, Sorbitan Sesquioleate, Phenoxyethanol, Triethoxycaprylylsilane, Iron Oxides(CI77491), Beeswax, Iron Oxides(CI77499), Aluminum Hydroxide, Ethylhexylglycerin, Fragrance, Adenosine, Silica dimethyl silylate, Disodium EDTA
- PURPOSE
- WARNINGS
- DESCRIPTION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEMATIS MORNING DEW BB 21 LIGHT BEIGE
titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71702-090 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) Titanium Dioxide 4.06 g in 50 mL Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate 3.50 g in 50 mL Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 2.00 g in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71702-090-02 1 in 1 CARTON 08/01/2017 1 NDC:71702-090-01 50 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 08/01/2017 Labeler - Coshub Co., Ltd. (689846820) Registrant - Coshub Co., Ltd. (689846820) Establishment Name Address ID/FEI Business Operations COSON Co., Ltd._Osan Plant 689847210 manufacture(71702-090)