Label: ERBORIAN CC DULL CORRECT SPF25- octinoxate, octisalate, titanium dioxide, zinc oxide cream
- NDC Code(s): 10345-914-15, 10345-914-45
- Packager: LABORATOIRES M&L
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 9, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
- Warnings
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Directions
For sunscreen use:
- Apply liberally 15 minutes before sun exposure
- Reapply at least every 2 hours
- Use a water resistant sunscreen if swimming or sweating
- 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 value of 15 or higher and other sun protection measures including: Sun Protection Measures.
- Limit time in the sun, especially from 10 a.m. –2 p.m.
- Wear long-sleeved shirts, pants, hats and sunglasses
- Children under 6 months of age: Ask a doctor
- Other information
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Inactive ingredients
AQUA/WATER - CYCLOMETHICONE - MICA - C12-15 ALKYL BENZOATE - DIPROPYLENE GLYCOL - GLYCERIN - CI 77891/TITANIUM DIOXIDE - PEG-10 DIMETHICONE - METHYL TRIMETHICONE - CI 77007/ULTRAMARINES - DIMETHICONE - BUTYLENE GLYCOL - DISTEARDIMONIUM HECTORITE - CI 77492/IRON OXIDES - MAGNESIUM SULFATE - CENTELLA ASIATICA EXTRACT - GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT - TALC - VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER - DIMETHICONE/ VINYL DIM E T H I C O N E CROSSPOLYMER - ALUMINUM HYDROXIDE - TRIHYDROXYSTEARIN - METHICONE - PALMITIC ACID - POLYESTER-1 - STEARIC ACID - SILICA DIMETHYL SILYLATE - TOCOPHERYL ACETATE - ETHYLHEXYLGLYCERIN - TIN OXIDE - PHENOXYETHANOL - PARFUM/FRAGRANCE - HEXYL CINNAMAL- ALPHA-ISOMETHYL IONONE - LINALOOL - CITRONELLOL - GERANIOL - EUGENOL - LIMONENE - CI 77491/IRON OXIDES - CI 77499/IRON OXIDES
- Questions or comments?
- Erborian – CC Dull Correct SPF25, 15mL (68021-914-15)
- Erborian – CC Dull Correct SPF25, 45mL (68021-914-45)
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INGREDIENTS AND APPEARANCE
ERBORIAN CC DULL CORRECT SPF25
octinoxate, octisalate, titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10345-914 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 OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 20 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 47 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 38.4 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE (UNII: NMQ347994Z) MICA (UNII: V8A1AW0880) DIPROPYLENE GLYCOL (UNII: E107L85C40) GLYCERIN (UNII: PDC6A3C0OX) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) ULTRAMARINE BLUE (UNII: I39WR998BI) DIMETHICONE (UNII: 92RU3N3Y1O) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) CENTELLA ASIATICA (UNII: 7M867G6T1U) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) TALC (UNII: 7SEV7J4R1U) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) TRIHYDROXYSTEARIN (UNII: 06YD7896S3) METHICONE (20 CST) (UNII: 6777U11MKT) PALMITIC ACID (UNII: 2V16EO95H1) STEARIC ACID (UNII: 4ELV7Z65AP) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) STANNIC OXIDE (UNII: KM7N50LOS6) PHENOXYETHANOL (UNII: HIE492ZZ3T) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) GERANIOL (UNII: L837108USY) EUGENOL (UNII: 3T8H1794QW) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10345-914-15 1 in 1 BOX 05/27/2019 1 15 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:10345-914-45 1 in 1 BOX 05/27/2019 2 45 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 Drug M020 05/27/2019 Labeler - LABORATOIRES M&L (262533623)