ERBORIAN - BB CREME AU GINSENG CARAMEL SPF20- octinoxate, titanium dioxide, zinc oxide cream 
LABORATOIRES M&L

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.

----------

ERBORIAN - BB CREME AU GINSENG CARAMEL SPF20

Drug Facts

Active ingredients

Ethylhexyl Methoxicynnamate / Octinoxate 3%
Titanium dioxide 6,28% 
Zinc oxide 1.92%

Purpose

Sunscreen

Uses

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:

Other information

Inactive ingredients

Aqua/water - cyclomethicone - glycerin - CI 77492/iron oxides - dipropylene glycol - peg-10 dimethicone - dimethicone - isoeicosane - talc - hexyl laurate - betaine - disteardimonium hectorite - panax ginseng root extract - kigelia africana fruit extract - portulaca oleracea extract - lycyrrhiza glabra (licorice) root extract - dioscorea villosa (wild yam) root extract - equisetum giganteum extract - glycosyl trehalose - palmitic acid - magnesium sulfate - aluminum hydroxide - dimethicone/vinyl dimethicone crosspolymer - acrylates/dimethicone copolymer - hydrogenated starch hydrolysate - stearic acid - methicone - phenoxyethanol - tocopheryl acetate - triethoxycaprylylsilane - parfum/fragrance - ethylhexylglycerin
- butylene glycol - hexyl cinnamal - citronellol - alpha-isomethyl ionone - linalool - geraniol - eugenol - limonene - CI 77499/iron oxides - CI 77491/iron oxides

Questions or comments?

Call toll free 1-888-975-2162

Package Labeling:

Label

ERBORIAN - BB CREME AU GINSENG CARAMEL SPF20 
octinoxate, titanium dioxide, zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10345-903
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE30 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE62.8 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION19.2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE (UNII: NMQ347994Z)  
GLYCERIN (UNII: PDC6A3C0OX)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ISOEICOSANE (UNII: AR294KAG3T)  
TALC (UNII: 7SEV7J4R1U)  
HEXYL LAURATE (UNII: 4CG9F9W01Q)  
BETAINE (UNII: 3SCV180C9W)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
ASIAN GINSENG (UNII: CUQ3A77YXI)  
KIGELIA AFRICANA FRUIT (UNII: L4J6XXD1E0)  
PURSLANE (UNII: M6S840WXG5)  
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)  
BEMISIOSE (UNII: 76B4LOB2YC)  
PALMITIC ACID (UNII: 2V16EO95H1)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
METHICONE (20 CST) (UNII: 6777U11MKT)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
GERANIOL (UNII: L837108USY)  
EUGENOL (UNII: 3T8H1794QW)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10345-903-151 in 1 BOX12/16/2016
115 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:10345-903-451 in 1 BOX12/16/2016
245 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35212/16/2016
Labeler - LABORATOIRES M&L (262533623)

Revised: 12/2020
Document Id: b7c7b19d-f686-5514-e053-2995a90aed92
Set id: 43c81760-6bb6-25fe-e054-00144ff8d46c
Version: 3
Effective Time: 20201231
 
LABORATOIRES M&L