Label: LBEL LIBERTAGE CC MATTE PERFECTIONING-EFFECT MOISTURIZING FACE SPF 30- octinoxate and zinc oxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 43596-0089-1, 43596-0089-2 - Packager: Ventura Corporation LTD
- 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 November 14, 2019
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
- Directions
- Other information
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Inactive ingredients
IISODODECANE, DIMETHICONE, WATER, POLYSILICONE-11, GLYCERIN, PEG-10 DIMETHICONE, ZEA MAYS (CORN) STARCH, TITANIUM DIOXIDE, HYDROXYETHYL UREA, IRON OXIDES, POLYMETHYLSILSESQUIOXANE, SODIUM PCA, PEG/PPG-18/18 DIMETHICONE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, PHENOXYETHANOL, METHYLPROPANEDIOL, TOCOPHERYL ACETATE, CAPRYLYL GLYCOL, DISTEARDIMONIUM HECTORITE, PEG-8, CHLORPHENESIN, SILANEDIOL SALICYLATE, CERAMIDE 3, TRIETHOXYCAPRYLYLSILANE, TROMETHAMINE, LAURETH-12, BUTYLENE GLYCOL, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, PPG-1-PEG-9 LAURYL GLYCOL ETHER, HEDERA HELIX (IVY) LEAF/STEM EXTRACT, PHYTIC ACID, SODIUM POLYACRYLATE.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 35 g Tube Box
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INGREDIENTS AND APPEARANCE
LBEL LIBERTAGE CC MATTE PERFECTIONING-EFFECT MOISTURIZING FACE SPF 30
octinoxate and zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0089 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g in 1 g Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 0.06 g in 1 g Inactive Ingredients Ingredient Name Strength ISODODECANE (UNII: A8289P68Y2) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) STARCH, CORN (UNII: O8232NY3SJ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) FERRIC OXIDE RED (UNII: 1K09F3G675) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYLPROPANEDIOL (UNII: N8F53B3R4R) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) CHLORPHENESIN (UNII: I670DAL4SZ) SILANEDIOL SALICYLATE (UNII: C054DF30K0) CERAMIDE NP (UNII: 4370DF050B) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) TROMETHAMINE (UNII: 023C2WHX2V) LAURETH-12 (UNII: OAH19558U1) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L) FYTIC ACID (UNII: 7IGF0S7R8I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0089-2 1 in 1 BOX 08/08/2018 1 NDC:43596-0089-1 35 g 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 final part352 08/08/2018 Labeler - Ventura Corporation LTD (602751344) Establishment Name Address ID/FEI Business Operations Bel Star S.A. (Colombia) 880160197 MANUFACTURE(43596-0089)