Label: ERBORIAN CC RED CORRECT SPF 25- octinoxate, octisalate, titanium dioxide, zinc oxide cream
- NDC Code(s): 10345-912-15, 10345-912-45
- Packager: Laboratoires M&L
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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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
- Sun Protection Meausres. Spending time in the sun incerases 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:
- 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 - Dipropylene Glycol - Glycerin - Peg-10 Dimethicone - Methyl Trimethicone - CI 77891/titanium Dioxide - C12-15 Alkyl Benzoate - Dimethicone - Vinyl Dimethicone/methicone Silsesquioxane Crosspolymer - Disteardimonium Hectorite - Magnesium Sulfate - Butylene Glycol - Centella Asiatica Extract - Talc - Dimethicone/Vinyl Dimethicone Crosspolymer - Aluminum Hydroxide - Trihydroxystearn - Phenoxyethanol - Mica - Methicone - Palmitic Acid - Stearic acid - Ethylhexylglycerin - Tocopheryl Acetate - Polyester-1 - Silica Dimethyl Silylate - Triethoxycaprylylsilane - Parfum/Fragrance - Hexyl Cinnamal - Alpha-Isomethyl Ionone - Linalool - Citronellol - Geraniol - Eugenol - Limonene - CI 77492/Iron Oxides - CI 77288/chormium Oxide Greens - CI 77491/Iron Oxides - CI77499/Iron Oxides
- Questions or comments?
- ERBORIAN - CC RED CORRECT SPF 25 15ml (10345-912-15)
- ERBORIAN - CC RED CORRECT SPF 25 45ml (10345-912-45)
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INGREDIENTS AND APPEARANCE
ERBORIAN CC RED CORRECT SPF 25
octinoxate, octisalate, titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10345-912 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 23.4 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 PHENOXYETHANOL (UNII: HIE492ZZ3T) MICA (UNII: V8A1AW0880) METHICONE (20 CST) (UNII: 6777U11MKT) PALMITIC ACID (UNII: 2V16EO95H1) STEARIC ACID (UNII: 4ELV7Z65AP) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLYESTER-10 (UNII: 212N9O2MMZ) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) LINALOOL, (+/-)- (UNII: D81QY6I88E) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) GERANIOL (UNII: L837108USY) EUGENOL (UNII: 3T8H1794QW) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) CHROMIC OXIDE (UNII: X5Z09SU859) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) WATER (UNII: 059QF0KO0R) CYCLOMETHICONE (UNII: NMQ347994Z) GLYCERIN (UNII: PDC6A3C0OX) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) DIMETHICONE (UNII: 92RU3N3Y1O) VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CENTELLA ASIATICA (UNII: 7M867G6T1U) TALC (UNII: 7SEV7J4R1U) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) TRIHYDROXYSTEARIN (UNII: 06YD7896S3) DIPROPYLENE GLYCOL (UNII: E107L85C40) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10345-912-15 1 in 1 BOX 07/01/2018 1 15 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:10345-912-45 1 in 1 BOX 07/01/2018 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 07/01/2018 Labeler - Laboratoires M&L (262533623)