ERBORIAN CC RED CORRECT COLOR CORRECTING SPF 25- octinoxate, octisalate, titanium dioxide, zinc oxide cream

ERBORIAN CC Red Correct Color Correcting SPF 25 by

Drug Labeling and Warnings

ERBORIAN CC Red Correct Color Correcting SPF 25 by is a Otc medication manufactured, distributed, or labeled by LABORATOIRES M&L. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Octinoxate 6.00%
Octisalate 2.00%
Titanium dioxide 2.34%
Zinc oxide 3.84%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Do not use

• on damaged or broken skin

When using this product

• keep out of eyes. Rinse with water to remove

Stop use and ask a doctor if

• rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

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

• Protect the product in this container from excessive heat and direct sun

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 - TRIHYDROXYSTEARIN - 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/CHROMIUM OXIDE GREENS - CI 77491/ IRON OXIDES - CI 77499/IRON OXIDES

Questions or comments?

Call toll free 1-866-464-3358

Package Labeling: 1.5 mL

Package Labeling: 5 mL

Package Labeling: 15 mL

Package Labeling: 45 mL

INGREDIENTS AND APPEARANCE

ERBORIAN CC RED CORRECT COLOR CORRECTING SPF 25 
octinoxate, octisalate, titanium dioxide, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10345-953
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (ETHYLHEXYL METHOXYCINNAMATE - UNII:4Y5P7MUD51)	OCTINOXATE	60 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	20 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (CI 77891 - 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
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE (UNII: NMQ347994Z)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERIN (UNII: PDC6A3C0OX)
METHYL TRIMETHICONE (UNII: S73ZQI0GXM)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
DIMETHICONE (UNII: 92RU3N3Y1O)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
MAGNESIUM SULFATE (UNII: DE08037SAB)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
TALC (UNII: 7SEV7J4R1U)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MICA (UNII: V8A1AW0880)
PALMITIC ACID (UNII: 2V16EO95H1)
STEARIC ACID (UNII: 4ELV7Z65AP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
CITRONELLOL (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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10345-953-01	1.5 mL in 1 PACKET; Type 0: Not a Combination Product	09/01/2025
2	NDC: 10345-953-05	1 in 1 BOX	09/01/2025
2		5 mL in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 10345-953-15	1 in 1 BOX	09/01/2025
3		15 mL in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 10345-953-45	1 in 1 BOX	09/01/2025
4		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	09/01/2025

Labeler - LABORATOIRES M&L (262533623)

Registrant - LABORATOIRES M&L (262533623)