Label: YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 1- octinoxate liquid
YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 3- octinoxate liquid
YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 4- octinoxate liquid
YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 2- octinoxate liquid
YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 5- octinoxate liquid
YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 7- octinoxate liquid
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NDC Code(s):
23319-0007-1,
23319-0008-1,
23319-0009-1,
23319-0010-1, view more23319-0011-1, 23319-0012-1
- Packager: Yanbal USA, Inc.
- Category: HUMAN OTC DRUG LABEL
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 May 19, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Uses
- Warnings
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Directions
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating or immediately after towel drying
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Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m.-2 p.m.
- wear long-sleeve shirts, pants, hats and sunglasses
- children under 6 months: Ask a doctor.
- Other information
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Inactive ingredients
WATER (AQUA), CYCLOPENTASILOXANE, ALCOHOL DENAT., ISONONYL ISONONANOATE, PEG-10 DIMETHICONE, BUTYLENE GLYCOL, KAOLIN, DIMETHICONE, DIMETHICONE/DIVINYLDIMETHICONE/SILSESQUIOXANE CROSSPOLYMER, MAGNESIUM SULFATE, TRIMETHYLSILOXYSILICATE, ALUMINUM STARCH OCTENYLSUCCINATE, DIPENTAERYTHRITYL TETRABEHENATE/POLYHYDROXYSTEARATE, SODIUM CHLORIDE, FRAGRANCE (PARFUM), DIMETHICONE/PEG-10/15 CROSSPOLYMER, SORBITAN SESQUIOLEATE, PHENOXYETHANOL, TRIETHOXYCAPRYLYLSILANE, DISTEARDIMONIUM HECTORITE, XANTHAN GUM, TRIFLUOROMETHYL C1-4 ALKYL DIMETHICONE, PROPYLENE CARBONATE, DISODIUM EDTA, CHLORPHENESIN, MYRICA PUBESCENS FRUIT WAX, RETINYL PALMITATE, ENANTIA CHLORANTHA BARK EXTRACT, OLEANOLIC ACID, MICA, IRON OXIDES (CI 77491/CI 77492/CI 77499), TITANIUM DIOXIDE (CI 77891).
- Company Information
- Product Packaging - Tono 1
- Product Packaging - Tono 2
- Product Packaging - Tono 3
- Product Packaging - Tono 4
- Product Packaging - Tono 5
- Product Packaging - Tono 7
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INGREDIENTS AND APPEARANCE
YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 1
octinoxate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:23319-0007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) MORELLA PUBESCENS FRUIT WAX (UNII: 2N43GS24LV) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHICONE (UNII: 92RU3N3Y1O) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) CHLORPHENESIN (UNII: I670DAL4SZ) FERROUS OXIDE (UNII: G7036X8B5H) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) KAOLIN (UNII: 24H4NWX5CO) MICA (UNII: V8A1AW0880) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) SODIUM CHLORIDE (UNII: 451W47IQ8X) PROPYLENE CARBONATE (UNII: 8D08K3S51E) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) ALCOHOL (UNII: 3K9958V90M) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23319-0007-1 1 in 1 CARTON 11/15/2018 1 27 mL in 1 BOTTLE; 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 11/15/2018 09/30/2024 YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 3
octinoxate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:23319-0009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength MICA (UNII: V8A1AW0880) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) SODIUM CHLORIDE (UNII: 451W47IQ8X) PROPYLENE CARBONATE (UNII: 8D08K3S51E) ALCOHOL (UNII: 3K9958V90M) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) MORELLA PUBESCENS FRUIT WAX (UNII: 2N43GS24LV) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) WATER (UNII: 059QF0KO0R) ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHICONE (UNII: 92RU3N3Y1O) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) CHLORPHENESIN (UNII: I670DAL4SZ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERROUS OXIDE (UNII: G7036X8B5H) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) KAOLIN (UNII: 24H4NWX5CO) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23319-0009-1 1 in 1 CARTON 11/15/2018 1 27 mL in 1 BOTTLE; 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 11/15/2018 09/30/2024 YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 4
octinoxate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:23319-0010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength MICA (UNII: V8A1AW0880) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) SODIUM CHLORIDE (UNII: 451W47IQ8X) PROPYLENE CARBONATE (UNII: 8D08K3S51E) ALCOHOL (UNII: 3K9958V90M) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) MORELLA PUBESCENS FRUIT WAX (UNII: 2N43GS24LV) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) WATER (UNII: 059QF0KO0R) ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHICONE (UNII: 92RU3N3Y1O) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) CHLORPHENESIN (UNII: I670DAL4SZ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERROUS OXIDE (UNII: G7036X8B5H) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) KAOLIN (UNII: 24H4NWX5CO) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23319-0010-1 1 in 1 CARTON 11/15/2018 04/01/2021 1 27 mL in 1 BOTTLE; 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 11/15/2018 04/01/2021 YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 2
octinoxate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:23319-0008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength MICA (UNII: V8A1AW0880) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) SODIUM CHLORIDE (UNII: 451W47IQ8X) PROPYLENE CARBONATE (UNII: 8D08K3S51E) ALCOHOL (UNII: 3K9958V90M) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) MORELLA PUBESCENS FRUIT WAX (UNII: 2N43GS24LV) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) WATER (UNII: 059QF0KO0R) ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHICONE (UNII: 92RU3N3Y1O) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) CHLORPHENESIN (UNII: I670DAL4SZ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERROUS OXIDE (UNII: G7036X8B5H) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) KAOLIN (UNII: 24H4NWX5CO) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23319-0008-1 1 in 1 CARTON 11/15/2018 1 27 mL in 1 BOTTLE; 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 11/15/2018 10/31/2024 YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 5
octinoxate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:23319-0011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength MICA (UNII: V8A1AW0880) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) SODIUM CHLORIDE (UNII: 451W47IQ8X) PROPYLENE CARBONATE (UNII: 8D08K3S51E) ALCOHOL (UNII: 3K9958V90M) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) MORELLA PUBESCENS FRUIT WAX (UNII: 2N43GS24LV) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) WATER (UNII: 059QF0KO0R) ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHICONE (UNII: 92RU3N3Y1O) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) CHLORPHENESIN (UNII: I670DAL4SZ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERROUS OXIDE (UNII: G7036X8B5H) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) KAOLIN (UNII: 24H4NWX5CO) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23319-0011-1 1 in 1 CARTON 11/15/2018 01/01/2021 1 27 mL in 1 BOTTLE; 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 11/15/2018 01/01/2021 YANBAL BASE LIQUIDA MATIFICANTE MATTIFYING FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 TONO 7
octinoxate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:23319-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength MICA (UNII: V8A1AW0880) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) SODIUM CHLORIDE (UNII: 451W47IQ8X) PROPYLENE CARBONATE (UNII: 8D08K3S51E) ALCOHOL (UNII: 3K9958V90M) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) MORELLA PUBESCENS FRUIT WAX (UNII: 2N43GS24LV) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) WATER (UNII: 059QF0KO0R) ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHICONE (UNII: 92RU3N3Y1O) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) CHLORPHENESIN (UNII: I670DAL4SZ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERROUS OXIDE (UNII: G7036X8B5H) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) KAOLIN (UNII: 24H4NWX5CO) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23319-0012-1 1 in 1 CARTON 11/15/2018 01/01/2021 1 27 mL in 1 BOTTLE; 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 11/15/2018 01/01/2021 Labeler - Yanbal USA, Inc. (001801369) Establishment Name Address ID/FEI Business Operations Yanbal de Colombia S.A.S. 880215657 manufacture(23319-0007, 23319-0008, 23319-0009, 23319-0010, 23319-0011, 23319-0012)