Label: ERBORIAN - CC CREME HIGH DEFINITION SPF 25- octinoxate, octisalate, titanium dioxide, zinc oxide cream
- NDC Code(s): 10345-910-01, 10345-910-05, 10345-910-15, 10345-910-45
- Packager: LABORATOIRES M&L
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
If you are a consumer or patient please visit this version.
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- 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 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 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 - C12-15 Alkyl Benzoate - Dimethicone - CI 77492/Iron Oxides - Disteardimonium Hectorite - Magnesium Sulfate - Vinyl Dimethicone/Methicone Silsesquioxane
Crosspolymer - Centella Asiatica Extract - Mel/Honey Extract - Mica - Talc - Trihydroxystearin - Butylene Glycol - Polyester-1 - Aluminum Hydroxide - Silica Dimethyl Silylate - Palmitic Acid - Stearic Acid - Tocopheryl Acetate - Ethylhexylglycerin - Phenoxyethanol - Methicone - Dimethicone/Vinyl Dimethicone Crosspolymer - Parfum/Fragrance - Hexyl Cinnamal - Alpha-Isomethyl Ionone - Linalool - Citronellol - Geraniol - Eugenol - Limonene - CI 77491/Iron Oxides - Questions or comments
- ERBORIAN - CC CREME HIGH DEFINITION SPF 25 5ml (10345-910-05)
- Product Label
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INGREDIENTS AND APPEARANCE
ERBORIAN - CC CREME HIGH DEFINITION SPF 25
octinoxate, octisalate, titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10345-910 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 20 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 60 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 49.7 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 19.2 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIPROPYLENE GLYCOL (UNII: E107L85C40) GLYCERIN (UNII: PDC6A3C0OX) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) CENTELLA ASIATICA (UNII: 7M867G6T1U) HONEY (UNII: Y9H1V576FH) MICA (UNII: V8A1AW0880) TALC (UNII: 7SEV7J4R1U) TRIHYDROXYSTEARIN (UNII: 06YD7896S3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) PALMITIC ACID (UNII: 2V16EO95H1) STEARIC ACID (UNII: 4ELV7Z65AP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) LINALOOL, (+/-)- (UNII: D81QY6I88E) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) 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:10345-910-15 1 in 1 BOX 02/06/2015 1 15 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:10345-910-01 1.5 mL in 1 PACKET; Type 0: Not a Combination Product 12/03/2017 3 NDC:10345-910-45 1 in 1 BOX 02/06/2015 3 45 mL in 1 TUBE; Type 0: Not a Combination Product 4 NDC:10345-910-05 1 in 1 BOX 07/01/2018 4 5 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 02/06/2015 Labeler - LABORATOIRES M&L (262533623)