Label: PUTTO SECRET SUN SCREEN- titanium dioxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 75885-020-01 - Packager: AGABANG & COMPANY
- 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 13, 2013
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Cyclopentasiloxane, Glechoma Hederacea Flower/Leaf/Stem Extract, Houttuynia Cordata Extract, Plantago Asiatica Extract, Cetearyl Alcohol, Ethylhexyl Methoxycinnamate, Propanediol, Dipropylene Glycol, Glycerin, Morus Alba Leaf Extract, Ulmus Davidiana Root Extract, Butylene Glycol, Octocrylene, Polysorbate 60, Polyglyceryl-3 Methylglucose Distearate, 1,2-Hexanediol, Alumina, Betaine, Hexyl Laurate, Methicone, PEG-10 Dimethicone, Sorbitan Olivate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Glyceryl Stearate, PEG-100 Stearate, Fragrance, Magnesium Aluminum Silicate, Caprylhydroxamic Acid, Caprylyl Glycol, Panthenol, Triethanolamine, Xanthan Gum, Disodium EDTA, Hydroxyethylcellulose, Tocopheryl Acetate, Beta-Glucan, Butyrospermum Parkii (Shea Butter), Ceramide 3, Squalane
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PUTTO SECRET SUN SCREEN
titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75885-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 6 mg in 100 mL Inactive Ingredients Ingredient Name Strength CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLECHOMA HEDERACEA FLOWERING TOP (UNII: 2458J91U39) HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22) PLANTAGO ASIATICA (UNII: 5F5728J5E8) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) OCTINOXATE (UNII: 4Y5P7MUD51) PROPANEDIOL (UNII: 5965N8W85T) DIPROPYLENE GLYCOL (UNII: E107L85C40) GLYCERIN (UNII: PDC6A3C0OX) MORUS ALBA LEAF (UNII: M8YIA49Q2P) ULMUS DAVIDIANA ROOT (UNII: URQ79U8261) POLYSORBATE 60 (UNII: CAL22UVI4M) OCTOCRYLENE (UNII: 5A68WGF6WM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75885-020-01 65 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 07/13/2013 Labeler - AGABANG & COMPANY (687808766) Registrant - AGABANG & COMPANY (687808766) Establishment Name Address ID/FEI Business Operations AGABANG & COMPANY 687808766 manufacture(75885-020)