Label: LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 LATTE 180-F- octinoxate, zinc oxide emulsion
LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 CHAMPAGNE 170-N- octinoxate, zinc oxide emulsion
LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 ALMENDRA 230-N- octinoxate, zinc oxide emulsion
LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 BEIGE 220-C- octinoxate, zinc oxide emulsion
LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 CAPUCCINO 310-C- octinoxate, zinc oxide emulsion
LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 MOKACCINO 390-N- octinoxate, zinc oxide emulsion
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NDC Code(s):
14141-017-01,
14141-018-01,
14141-019-01,
14141-020-01, view more14141-021-01, 14141-022-01
- Packager: Bel Star S.A.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 26, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions
- Other information
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Inactive ingredients
DIMETHICONE, ISODODECANE, WATER, MICA, GLYCERIN, TRIMETHYLSILOXYSILICATE, PEG-10 DIMETHICONE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, ALCOHOL DENAT., HYDROXYETHYL UREA, PEG/PPG-18/18 DIMETHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, SODIUM PCA, POLYSILICONE-11, SILICA, LECITHIN, PHENOXYETHANOL, SODIUM CHLORIDE, NIACINAMIDE, SILICA DIMETHYL SILYLATE, TRIETHOXYCAPRYLYLSILANE, CAPRYLYL GLYCOL, DISTEARDIMONIUM HECTORITE, CHLORPHENESIN, FRAGRANCE, PANTHENOL, TOCOPHERYL ACETATE, SACCHAROMYCES LYSATE, PERFLUOROHEXYLETHYL TRIETHOXYSILANE, DISODIUM SUCCINATE, GLUTAMIC ACID, GLYCINE, THREONINE, VALINE. MAY CONTAIN: TITANIUM DIOXIDE, IRON OXIDES.
- Company Information
- Product Packaging ALMENDRA 230-N
- Product Packaging BEIGE 220-C
- Product Packaging CAPUCCINO 310-C
- Product Packaging CHAMPAGNE 170-N
- Product Packaging LATTE 180-F
- Product Packaging MOKACCINO 390-N
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INGREDIENTS AND APPEARANCE
LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 LATTE 180-F
octinoxate, zinc oxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14141-021 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 29.4 mg in 1 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SACCHAROMYCES LYSATE (UNII: R85W246Z1C) THREONINE (UNII: 2ZD004190S) WATER (UNII: 059QF0KO0R) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PANTHENOL (UNII: WV9CM0O67Z) VALINE (UNII: HG18B9YRS7) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) ALCOHOL (UNII: 3K9958V90M) SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3) GLUTAMIC ACID (UNII: 3KX376GY7L) GLYCINE (UNII: TE7660XO1C) CHLORPHENESIN (UNII: I670DAL4SZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) SODIUM CHLORIDE (UNII: 451W47IQ8X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) FERRIC OXIDE RED (UNII: 1K09F3G675) NIACINAMIDE (UNII: 25X51I8RD4) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ISODODECANE (UNII: A8289P68Y2) MICA (UNII: V8A1AW0880) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14141-021-01 1 in 1 BOX 01/19/2022 1 26 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/19/2022 LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 CHAMPAGNE 170-N
octinoxate, zinc oxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14141-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 29.4 mg in 1 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SACCHAROMYCES LYSATE (UNII: R85W246Z1C) THREONINE (UNII: 2ZD004190S) WATER (UNII: 059QF0KO0R) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PANTHENOL (UNII: WV9CM0O67Z) VALINE (UNII: HG18B9YRS7) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) ALCOHOL (UNII: 3K9958V90M) SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3) GLUTAMIC ACID (UNII: 3KX376GY7L) GLYCINE (UNII: TE7660XO1C) CHLORPHENESIN (UNII: I670DAL4SZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) SODIUM CHLORIDE (UNII: 451W47IQ8X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) FERRIC OXIDE RED (UNII: 1K09F3G675) NIACINAMIDE (UNII: 25X51I8RD4) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ISODODECANE (UNII: A8289P68Y2) MICA (UNII: V8A1AW0880) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14141-020-01 1 in 1 BOX 01/19/2022 1 26 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/19/2022 LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 ALMENDRA 230-N
octinoxate, zinc oxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14141-017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 29.4 mg in 1 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SACCHAROMYCES LYSATE (UNII: R85W246Z1C) THREONINE (UNII: 2ZD004190S) VALINE (UNII: HG18B9YRS7) WATER (UNII: 059QF0KO0R) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PANTHENOL (UNII: WV9CM0O67Z) GLYCINE (UNII: TE7660XO1C) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) ALCOHOL (UNII: 3K9958V90M) SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3) GLUTAMIC ACID (UNII: 3KX376GY7L) CHLORPHENESIN (UNII: I670DAL4SZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) SODIUM CHLORIDE (UNII: 451W47IQ8X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) FERRIC OXIDE RED (UNII: 1K09F3G675) NIACINAMIDE (UNII: 25X51I8RD4) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) ISODODECANE (UNII: A8289P68Y2) MICA (UNII: V8A1AW0880) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14141-017-01 1 in 1 BOX 01/19/2022 1 26 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/19/2022 LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 BEIGE 220-C
octinoxate, zinc oxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14141-018 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 29.4 mg in 1 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SACCHAROMYCES LYSATE (UNII: R85W246Z1C) THREONINE (UNII: 2ZD004190S) WATER (UNII: 059QF0KO0R) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PANTHENOL (UNII: WV9CM0O67Z) VALINE (UNII: HG18B9YRS7) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) ALCOHOL (UNII: 3K9958V90M) SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3) GLUTAMIC ACID (UNII: 3KX376GY7L) GLYCINE (UNII: TE7660XO1C) CHLORPHENESIN (UNII: I670DAL4SZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) SODIUM CHLORIDE (UNII: 451W47IQ8X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) FERRIC OXIDE RED (UNII: 1K09F3G675) NIACINAMIDE (UNII: 25X51I8RD4) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ISODODECANE (UNII: A8289P68Y2) MICA (UNII: V8A1AW0880) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14141-018-01 1 in 1 BOX 01/19/2022 1 26 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/19/2022 LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 CAPUCCINO 310-C
octinoxate, zinc oxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14141-019 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 29.4 mg in 1 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SACCHAROMYCES LYSATE (UNII: R85W246Z1C) THREONINE (UNII: 2ZD004190S) WATER (UNII: 059QF0KO0R) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PANTHENOL (UNII: WV9CM0O67Z) VALINE (UNII: HG18B9YRS7) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) ALCOHOL (UNII: 3K9958V90M) SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3) GLUTAMIC ACID (UNII: 3KX376GY7L) GLYCINE (UNII: TE7660XO1C) CHLORPHENESIN (UNII: I670DAL4SZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) SODIUM CHLORIDE (UNII: 451W47IQ8X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) FERRIC OXIDE RED (UNII: 1K09F3G675) NIACINAMIDE (UNII: 25X51I8RD4) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ISODODECANE (UNII: A8289P68Y2) MICA (UNII: V8A1AW0880) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14141-019-01 1 in 1 BOX 01/19/2022 1 26 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/19/2022 LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 MOKACCINO 390-N
octinoxate, zinc oxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14141-022 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 29.4 mg in 1 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SACCHAROMYCES LYSATE (UNII: R85W246Z1C) THREONINE (UNII: 2ZD004190S) WATER (UNII: 059QF0KO0R) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PANTHENOL (UNII: WV9CM0O67Z) VALINE (UNII: HG18B9YRS7) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) ALCOHOL (UNII: 3K9958V90M) SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3) GLUTAMIC ACID (UNII: 3KX376GY7L) GLYCINE (UNII: TE7660XO1C) CHLORPHENESIN (UNII: I670DAL4SZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) SODIUM CHLORIDE (UNII: 451W47IQ8X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) FERRIC OXIDE RED (UNII: 1K09F3G675) NIACINAMIDE (UNII: 25X51I8RD4) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ISODODECANE (UNII: A8289P68Y2) MICA (UNII: V8A1AW0880) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14141-022-01 1 in 1 BOX 01/19/2022 1 26 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/19/2022 Labeler - Bel Star S.A. (880160197)