Label: ERBORIAN - BB CREME AU GINSENG CLAIR SPF 20- octinoxate, titanium dioxide, zinc oxide cream
- NDC Code(s): 10345-900-15, 10345-900-45
- Packager: LABORATOIRES M&L
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 1, 2024
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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 - glycerin - peg-10 dimethicone - dipropylene glycol - dimethicone - talc - isoeicosane - hexyl laurate - disteardimonium hectorite - betaine - panax ginseng root extract - glycyrrhiza glabra (licorice) root extract - portulaca oleracea extract -
dioscorea villosa (wild yam) root extract - equisetum giganteum extract - kigelia africana fruit extract - hydrogenated starch hydrolysate
- ethylhexylglycerin - tocopheryl acetate - magnesium sulfate - silica - glycosyl trehalose - aluminum hydroxide - palmitic acid - stearic acid - phenoxyethanol - butylene glycol - acrylates/dimethicone copolymer - dimethicone/vinyl dimethicone crosspolymer - methicone - vinyl dimethicone/methicone silsesquioxane crosspolymer - parfum/fragrance - alpha-isomethyl ionone - hexyl cinnamal - linalool - citronellol - geraniol - eugenol - limonene - CI 77492/iron oxides - CI 77499/iron oxides - Questions or comments?
- Product Label
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INGREDIENTS AND APPEARANCE
ERBORIAN - BB CREME AU GINSENG CLAIR SPF 20
octinoxate, titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10345-900 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 30 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 62.8 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 ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) PALMITIC ACID (UNII: 2V16EO95H1) STEARIC ACID (UNII: 4ELV7Z65AP) PHENOXYETHANOL (UNII: HIE492ZZ3T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) GERANIOL (UNII: L837108USY) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE RED (UNII: 1K09F3G675) WATER (UNII: 059QF0KO0R) CYCLOMETHICONE (UNII: NMQ347994Z) GLYCERIN (UNII: PDC6A3C0OX) DIPROPYLENE GLYCOL (UNII: E107L85C40) DIMETHICONE (UNII: 92RU3N3Y1O) TALC (UNII: 7SEV7J4R1U) ISOEICOSANE (UNII: AR294KAG3T) HEXYL LAURATE (UNII: 4CG9F9W01Q) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) BETAINE (UNII: 3SCV180C9W) ASIAN GINSENG (UNII: CUQ3A77YXI) LICORICE (UNII: 61ZBX54883) PURSLANE (UNII: M6S840WXG5) KIGELIA AFRICANA FRUIT (UNII: L4J6XXD1E0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10345-900-15 1 in 1 BOX 02/06/2015 1 15 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:10345-900-45 1 in 1 BOX 02/06/2015 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 02/06/2015 Labeler - LABORATOIRES M&L (262533623)